{"id":2229,"date":"2026-08-26T03:29:49","date_gmt":"2026-08-26T03:29:49","guid":{"rendered":"https:\/\/supplierally.com\/uncategorized\/china-supplier-serial-number-allocation-records\/"},"modified":"2026-08-26T03:29:49","modified_gmt":"2026-08-26T03:29:49","slug":"china-supplier-serial-number-allocation-records","status":"publish","type":"post","link":"https:\/\/supplierally.com\/es\/uncategorized\/china-supplier-serial-number-allocation-records\/","title":{"rendered":"How to Require Unit Serial-Number Allocation Records From China Suppliers"},"content":{"rendered":"<p>A serial number can appear correct on one unit and still create a serious operational problem. The factory may apply the same number twice, skip an issued range, replace a damaged label without recording the old number, pack a serial range into the wrong shipment, or remove a reworked unit from a carton list without changing the serial record. A buyer needs an allocation record that connects each identifier to the approved product scope and its current status.<\/p>\n<p><strong>China supplier serial number allocation records<\/strong> are controlled records that show which unit identifiers were issued to a supplier, applied to a defined product scope, scanned or checked, packed, held, voided, reworked, or left unused. They can link a serial range or file to the buyer product ID, revision, work order, lot where relevant, carton or pallet range, and partial-shipment allocation. They do not prove a number is unique, compliant, authentic, warranty eligible, readable, linked to a particular end customer, or fit for a regulatory system.<\/p>\n<p>FDA&#8217;s UDI system applies to medical devices, not ordinary goods. Its structure is still useful for identifying the difference between a fixed product identifier and variable production information such as a lot, serial number, expiration date, or manufacturing date.<a href=\"https:\/\/www.fda.gov\/medical-devices\/unique-device-identification-system-udi-system\/udi-basics\" title=\"U.S. Food and Drug Administration, UDI Basics\" target=\"_blank\" rel=\"noopener\">1<\/a> Current 21 CFR Part 830 says a device identifier is used for one version or model and that a discontinued device identifier may not be reassigned to another device.<a href=\"https:\/\/www.ecfr.gov\/current\/title-21\/chapter-I\/subchapter-H\/part-830\" title=\"Electronic Code of Federal Regulations, 21 CFR Part 830 Unique Device Identification\" target=\"_blank\" rel=\"noopener\">2<\/a> FDA also explains that device labels may carry human-readable and machine-readable identification in its regulated context.<a href=\"https:\/\/www.fda.gov\/medical-devices\/device-advice-comprehensive-regulatory-assistance\/unique-device-identification-system-udi-system\" title=\"U.S. Food and Drug Administration, Unique Device Identification System\" target=\"_blank\" rel=\"noopener\">3<\/a> These sources do not create a serial-number system for general China sourcing. They support a buyer discipline: define which identifier applies to a product baseline, control issuance and reuse, capture exceptions, and reconcile identifiers to production and shipment records before handover.<\/p>\n<h2>Define the serial-number baseline<\/h2>\n<p>A serial number is not the same as a SKU, lot number, barcode, carton number, or shipping label. The buyer should define the purpose and scope of each identifier before a supplier prints or encodes anything.<\/p>\n<table>\n<thead>\n<tr>\n<th>Identifier<\/th>\n<th>Buyer purpose<\/th>\n<th>Keep separate from<\/th>\n<\/tr>\n<\/thead>\n<tbody>\n<tr>\n<td>Product ID or SKU<\/td>\n<td>Identifies approved product model or style<\/td>\n<td>Individual unit serial number<\/td>\n<\/tr>\n<tr>\n<td>Product revision<\/td>\n<td>Identifies controlled configuration<\/td>\n<td>Shipment or carton number<\/td>\n<\/tr>\n<tr>\n<td>Lot or batch<\/td>\n<td>Groups units produced under defined conditions<\/td>\n<td>Unit-level identifier<\/td>\n<\/tr>\n<tr>\n<td>Unit serial number<\/td>\n<td>Identifies one defined unit within buyer system<\/td>\n<td>Retail barcode alone<\/td>\n<\/tr>\n<tr>\n<td>Carton number<\/td>\n<td>Identifies shipping package in a range<\/td>\n<td>Individual unit serial number<\/td>\n<\/tr>\n<tr>\n<td>Pallet or logistics ID<\/td>\n<td>Identifies unitized load<\/td>\n<td>Product identifier<\/td>\n<\/tr>\n<tr>\n<td>Manufacturing date<\/td>\n<td>Identifies date scope where used<\/td>\n<td>Serial-number sequence<\/td>\n<\/tr>\n<tr>\n<td>Warranty or customer ID<\/td>\n<td>Supports separate commercial program<\/td>\n<td>Supplier production record<\/td>\n<\/tr>\n<\/tbody>\n<\/table>\n<p>The serial baseline should state the product ID and revision, serial format or buyer-controlled serial file, issuance source, range or allocation size, and whether the supplier may generate new numbers. It should also identify numbers that must never be reused, even if a unit is damaged, rejected, or removed from packing.<\/p>\n<h2>Issue a bounded range or controlled serial file<\/h2>\n<p>Do not ask a supplier to use &#8220;the correct serial numbers&#8221; without defining what it received. Issue one bounded range or controlled file per work order, lot, or another agreed scope. Record the allocation ID and the system or person who issued it.<\/p>\n<table>\n<thead>\n<tr>\n<th>Allocation field<\/th>\n<th>Evidence<\/th>\n<th>Buyer question<\/th>\n<\/tr>\n<\/thead>\n<tbody>\n<tr>\n<td>Allocation ID<\/td>\n<td>Buyer or supplier controlled reference<\/td>\n<td>Which record governs this range?<\/td>\n<\/tr>\n<tr>\n<td>Product and revision<\/td>\n<td>Approved product baseline<\/td>\n<td>Which configuration can use the numbers?<\/td>\n<\/tr>\n<tr>\n<td>Start and end serial<\/td>\n<td>Range record or file hash where appropriate<\/td>\n<td>What exact numbers were issued?<\/td>\n<\/tr>\n<tr>\n<td>Count issued<\/td>\n<td>Number of identifiers in scope<\/td>\n<td>Does the range size match planned production?<\/td>\n<\/tr>\n<tr>\n<td>Work order or lot<\/td>\n<td>Traveler or production reference<\/td>\n<td>Where can this range be used?<\/td>\n<\/tr>\n<tr>\n<td>Supplier site and line<\/td>\n<td>Factory and defined operation<\/td>\n<td>Who controls application?<\/td>\n<\/tr>\n<tr>\n<td>Issuance date<\/td>\n<td>Controlled record date<\/td>\n<td>When did the supplier receive the range?<\/td>\n<\/tr>\n<tr>\n<td>Supplier owner<\/td>\n<td>Named role or system owner<\/td>\n<td>Who can explain exceptions?<\/td>\n<\/tr>\n<tr>\n<td>Reuse rule<\/td>\n<td>Buyer instruction<\/td>\n<td>What happens to a voided number?<\/td>\n<\/tr>\n<\/tbody>\n<\/table>\n<p>The buyer can send a serial file, authorize a system integration, or ask the supplier to generate numbers under an agreed algorithm. The method matters less than the record. The buyer should know the source system, the exact scope, and the rule for numbers that do not end up on shippable units.<\/p>\n<h2>Track each status without hiding exceptions<\/h2>\n<p>Serial control breaks down when every issued number is marked &#8220;used&#8221; even though units were held, damaged, reworked, or never completed. Use statuses that describe what the supplier has done. The status does not decide final acceptance.<\/p>\n<table>\n<thead>\n<tr>\n<th>Status<\/th>\n<th>Meaning in buyer review<\/th>\n<\/tr>\n<\/thead>\n<tbody>\n<tr>\n<td>Issued<\/td>\n<td>Number belongs to defined supplier allocation<\/td>\n<\/tr>\n<tr>\n<td>Unused<\/td>\n<td>Number remains in allocation but has not been applied<\/td>\n<\/tr>\n<tr>\n<td>Printed or encoded<\/td>\n<td>Supplier reports number placed on label, marking, or system<\/td>\n<\/tr>\n<tr>\n<td>Applied<\/td>\n<td>Supplier reports number attached to a defined unit<\/td>\n<\/tr>\n<tr>\n<td>Scan or check complete<\/td>\n<td>Supplier completed the defined verification step<\/td>\n<\/tr>\n<tr>\n<td>Packed<\/td>\n<td>Supplier links unit serial to package or shipment scope<\/td>\n<\/tr>\n<tr>\n<td>Held<\/td>\n<td>Unit or number is restricted pending a decision<\/td>\n<\/tr>\n<tr>\n<td>Rework pending<\/td>\n<td>Unit is in a controlled rework path<\/td>\n<\/tr>\n<tr>\n<td>Voided<\/td>\n<td>Number must not be used on another unit<\/td>\n<\/tr>\n<tr>\n<td>Damaged label<\/td>\n<td>Unit or label requires controlled replacement record<\/td>\n<\/tr>\n<tr>\n<td>Duplicate suspected<\/td>\n<td>Same number appears in more than one record<\/td>\n<\/tr>\n<tr>\n<td>Missing or unreadable<\/td>\n<td>Expected number cannot be confirmed in defined evidence<\/td>\n<\/tr>\n<\/tbody>\n<\/table>\n<p>A voided number should remain in the record. It is not a blank space that the supplier can quietly assign to another unit. If the buyer permits a label replacement, the supplier should preserve the old number, new number if one is used, reason, date, and evidence link.<\/p>\n<h2>Reconcile serials to production and packing scope<\/h2>\n<p>A range allocation is only the start. The buyer should request a reconciliation that relates issued numbers to actual unit and shipment status. Use the same product revision and avoid comparing serial count to carton count without a stated pack-out relationship.<\/p>\n<table>\n<thead>\n<tr>\n<th>Reconciliation point<\/th>\n<th>Compare<\/th>\n<th>Escalate when<\/th>\n<\/tr>\n<\/thead>\n<tbody>\n<tr>\n<td>Issued range to applied count<\/td>\n<td>Allocation record to supplier application record<\/td>\n<td>Numbers fall outside range<\/td>\n<\/tr>\n<tr>\n<td>Applied to voided<\/td>\n<td>Unit status to exception log<\/td>\n<td>Number appears in both states<\/td>\n<\/tr>\n<tr>\n<td>Product revision to serial<\/td>\n<td>Product baseline to serial record<\/td>\n<td>Number is used on another revision<\/td>\n<\/tr>\n<tr>\n<td>Serial to work order<\/td>\n<td>Unit record to traveler or production record<\/td>\n<td>Unit is outside agreed production scope<\/td>\n<\/tr>\n<tr>\n<td>Serial to lot where used<\/td>\n<td>Identifier record to lot or batch record<\/td>\n<td>Lot relationship is missing or changed<\/td>\n<\/tr>\n<tr>\n<td>Serial to carton<\/td>\n<td>Unit record to carton or package range<\/td>\n<td>Unit is packed in another shipment scope<\/td>\n<\/tr>\n<tr>\n<td>Serial to partial shipment<\/td>\n<td>Allocation record to shipment release record<\/td>\n<td>Same serial appears in two releases<\/td>\n<\/tr>\n<tr>\n<td>Scan result to text record<\/td>\n<td>Scan export to serial list<\/td>\n<td>Unreadable, missing, or unexpected data appears<\/td>\n<\/tr>\n<\/tbody>\n<\/table>\n<p>This reconciliation does not prove the unit itself conforms. It shows whether the buyer&#8217;s serial-control data, supplier production scope, and packing evidence refer to the same stated units.<\/p>\n<h2>Keep serial numbers connected to carton and shipment records<\/h2>\n<p>A serialized product can be packed in a master carton, split between cartons, reworked after packing, or transferred to a different partial shipment. The supplier needs a controlled link among serial number, package, and allocation. This is more useful than a photograph of one label.<\/p>\n<table>\n<thead>\n<tr>\n<th>Physical movement<\/th>\n<th>Record link needed<\/th>\n<th>Buyer boundary<\/th>\n<\/tr>\n<\/thead>\n<tbody>\n<tr>\n<td>Unit packed<\/td>\n<td>Serial, carton number, packing date, and packing record<\/td>\n<td>Does not prove cargo handover<\/td>\n<\/tr>\n<tr>\n<td>Carton repacked<\/td>\n<td>Original and new carton relationship<\/td>\n<td>Does not prove unit condition<\/td>\n<\/tr>\n<tr>\n<td>Unit removed from carton<\/td>\n<td>Serial, reason, new status, and carton update<\/td>\n<td>Does not approve rework<\/td>\n<\/tr>\n<tr>\n<td>Serial range split between shipments<\/td>\n<td>Each serial to partial-shipment allocation<\/td>\n<td>Does not decide shipping release<\/td>\n<\/tr>\n<tr>\n<td>Palletized cargo<\/td>\n<td>Serial or carton-to-pallet relationship where agreed<\/td>\n<td>Does not prove pallet count<\/td>\n<\/tr>\n<tr>\n<td>Label replaced<\/td>\n<td>Old serial or label status, replacement record, and evidence<\/td>\n<td>Does not prove authenticity<\/td>\n<\/tr>\n<tr>\n<td>Shipment held<\/td>\n<td>Serial and package scope under hold<\/td>\n<td>Does not decide disposition<\/td>\n<\/tr>\n<tr>\n<td>Supplier handover<\/td>\n<td>Allocation and package record at handover<\/td>\n<td>Does not prove carrier custody<\/td>\n<\/tr>\n<\/tbody>\n<\/table>\n<p>FDA&#8217;s device UDI system uses a production identifier that can include a serial number in medical-device context.<a href=\"https:\/\/www.fda.gov\/medical-devices\/unique-device-identification-system-udi-system\/udi-basics\" title=\"U.S. Food and Drug Administration, UDI Basics\" target=\"_blank\" rel=\"noopener\">1<\/a> For a general buyer control, use the same practical separation: product model information, production information, and package logistics data should not be collapsed into one identifier unless the buyer&#8217;s system is designed to do so.<\/p>\n<h2>Preserve an exception log<\/h2>\n<p>Exceptions are expected in real production. A label can tear. A unit can fail a test. A carton can be repacked. The control is not to pretend these events did not happen. The control is to retain the original serial status and link it to the final outcome.<\/p>\n<table>\n<thead>\n<tr>\n<th>Exception<\/th>\n<th>Evidence to retain<\/th>\n<th>Final status<\/th>\n<\/tr>\n<\/thead>\n<tbody>\n<tr>\n<td>Duplicate serial<\/td>\n<td>Both records, source, date, and containment action<\/td>\n<td>Voided, corrected, or open<\/td>\n<\/tr>\n<tr>\n<td>Serial outside range<\/td>\n<td>Serial value, allocation reference, and supplier explanation<\/td>\n<td>Corrected or open<\/td>\n<\/tr>\n<tr>\n<td>Unreadable serial<\/td>\n<td>Photo or scan result and replacement evidence<\/td>\n<td>Replaced, voided, or held<\/td>\n<\/tr>\n<tr>\n<td>Unit rejected<\/td>\n<td>Serial, defect or hold record, and disposition link<\/td>\n<td>Held, reworked, or voided<\/td>\n<\/tr>\n<tr>\n<td>Unit reworked<\/td>\n<td>Serial, authorization, and verification status<\/td>\n<td>Pending or updated status<\/td>\n<\/tr>\n<tr>\n<td>Carton mismatch<\/td>\n<td>Serial and original\/new carton records<\/td>\n<td>Corrected or open<\/td>\n<\/tr>\n<tr>\n<td>Missing serial<\/td>\n<td>Expected scope and search evidence<\/td>\n<td>Open or voided under agreement<\/td>\n<\/tr>\n<tr>\n<td>Unused range remainder<\/td>\n<td>Allocation count and unused identifiers<\/td>\n<td>Retained, returned, or voided<\/td>\n<\/tr>\n<\/tbody>\n<\/table>\n<p>Do not delete a duplicate or voided line because it makes the final count look cleaner. A complete record gives a buyer a better basis for determining whether the supplier investigated the specific exception.<\/p>\n<h2>Separate serial control from compliance and warranty decisions<\/h2>\n<p>Serial-number data can support operations, but it does not carry every conclusion a buyer might want. Keep its role limited.<\/p>\n<table>\n<thead>\n<tr>\n<th>Topic<\/th>\n<th>Serial record can support<\/th>\n<th>It cannot establish alone<\/th>\n<\/tr>\n<\/thead>\n<tbody>\n<tr>\n<td>Unit identification<\/td>\n<td>Supplier-stated link between unit and record<\/td>\n<td>Authenticity or anti-counterfeit status<\/td>\n<\/tr>\n<tr>\n<td>Packing check<\/td>\n<td>Link to carton or shipment scope<\/td>\n<td>Cargo contents or carrier custody<\/td>\n<\/tr>\n<tr>\n<td>Rework follow-up<\/td>\n<td>Unit history and current status<\/td>\n<td>Product conformity<\/td>\n<\/tr>\n<tr>\n<td>Customer service<\/td>\n<td>Identifier lookup record<\/td>\n<td>Warranty eligibility<\/td>\n<\/tr>\n<tr>\n<td>Compliance documentation<\/td>\n<td>An input to qualified review<\/td>\n<td>Regulatory identification compliance<\/td>\n<\/tr>\n<tr>\n<td>Production control<\/td>\n<td>Allocation and exception visibility<\/td>\n<td>Process capability<\/td>\n<\/tr>\n<tr>\n<td>Shipment review<\/td>\n<td>Which serials are stated in a release<\/td>\n<td>Final shipment authorization<\/td>\n<\/tr>\n<tr>\n<td>Recall or traceability program<\/td>\n<td>One evidence element where required<\/td>\n<td>Regulatory recall readiness<\/td>\n<\/tr>\n<\/tbody>\n<\/table>\n<p>Use qualified product, regulatory, warranty, cybersecurity, and legal owners for their decisions. The supplier serial log should record facts, status, and evidence rather than certify an outcome.<\/p>\n<h2>Supplier request wording and FAQ<\/h2>\n<blockquote>\n<p>For [product ID and revision, work order or lot, supplier site, serial allocation ID, issued range or serial file, and intended shipment scope], provide a serial-number allocation and reconciliation record. Identify each number&#8217;s status as unused, printed or encoded, applied, scan checked, packed, held, rework pending, voided, damaged, duplicate suspected, or missing. Link each serial or defined range to the product revision, production record, lot where applicable, carton or package record, partial shipment allocation, and exception log. Preserve original and final status for replacements, duplicate findings, rework, holds, removed units, and unused numbers. Buyer review does not establish uniqueness, authenticity, warranty eligibility, regulatory identification compliance, product conformity, cargo contents, or shipment release.<\/p>\n<\/blockquote>\n<h2>What are China supplier serial number allocation records?<\/h2>\n<p>They are records showing which unit serial numbers were issued to a supplier and what happened to them during production, packing, and shipment preparation. They connect an identifier to the correct product scope, status, and exception record.<\/p>\n<h2>Is a serial number the same as a lot number?<\/h2>\n<p>No. A lot groups units produced under a defined scope. A serial number identifies one defined unit. A buyer can link both records when the product or program requires it, but they have different purposes.<\/p>\n<h2>What should happen to a serial number on a rejected unit?<\/h2>\n<p>The supplier should retain the serial in the record, link it to the hold, defect, rework, or disposal status, and follow the buyer&#8217;s defined reuse rule. Do not silently reuse it.<\/p>\n<h2>Do serial-number records prove that products are authentic?<\/h2>\n<p>No. The records show the supplier&#8217;s stated identifier allocation and status. Authenticity and anti-counterfeit decisions require separate source, testing, and qualified review processes.<\/p>\n<h2>Should a buyer require a scan of every serial number?<\/h2>\n<p>That depends on product risk, buyer system, and agreement. Define the evidence method, scope, and exception handling before production. A scan can improve reconciliation, but it does not replace other controls.<\/p>\n<h2>Keep unit identifiers visible through handover<\/h2>\n<p><strong>China supplier serial number allocation records<\/strong> give buyers a way to follow unit identifiers from issuance through production, packing, exceptions, and shipment allocation. The supplier records the product baseline, issued range, status changes, carton links, and voided or missing numbers. The buyer can then distinguish a complete serial record from a list that only looks complete.<\/p>\n<p>Start with one serialized product and one work order. Agree the issued range or file, status definitions, exception log, carton link, and partial-shipment record before the supplier applies the first label. That prevents a damaged label, reworked unit, or split shipment from creating an unexplained serial-number gap.<\/p>\n<p>Supplier Ally can help buyers organize supplier serial logs, product and packing records, exception follow-up, shipment allocation evidence, and factory communication. For regulatory, product, cybersecurity, warranty, legal, engineering, or final release decisions, use the appropriate qualified owner before acting.<\/p>\n<h2>References<\/h2>\n","protected":false},"excerpt":{"rendered":"<p>Require China supplier serial number allocation records to control issued, applied, packed, held, voided, and reconciled unit identifiers before handover.<\/p>","protected":false},"author":1,"featured_media":0,"comment_status":"open","ping_status":"open","sticky":false,"template":"","format":"standard","meta":{"_uag_custom_page_level_css":"","site-sidebar-layout":"default","site-content-layout":"","ast-site-content-layout":"default","site-content-style":"default","site-sidebar-style":"default","ast-global-header-display":"","ast-banner-title-visibility":"","ast-main-header-display":"","ast-hfb-above-header-display":"","ast-hfb-below-header-display":"","ast-hfb-mobile-header-display":"","site-post-title":"","ast-breadcrumbs-content":"","ast-featured-img":"","footer-sml-layout":"","theme-transparent-header-meta":"","adv-header-id-meta":"","stick-header-meta":"","header-above-stick-meta":"","header-main-stick-meta":"","header-below-stick-meta":"","astra-migrate-meta-layouts":"default","ast-page-background-enabled":"default","ast-page-background-meta":{"desktop":{"background-color":"var(--ast-global-color-5)","background-image":"","background-repeat":"repeat","background-position":"center center","background-size":"auto","background-attachment":"scroll","background-type":"","background-media":"","overlay-type":"","overlay-color":"","overlay-opacity":"","overlay-gradient":""},"tablet":{"background-color":"","background-image":"","background-repeat":"repeat","background-position":"center center","background-size":"auto","background-attachment":"scroll","background-type":"","background-media":"","overlay-type":"","overlay-color":"","overlay-opacity":"","overlay-gradient":""},"mobile":{"background-color":"","background-image":"","background-repeat":"repeat","background-position":"center center","background-size":"auto","background-attachment":"scroll","background-type":"","background-media":"","overlay-type":"","overlay-color":"","overlay-opacity":"","overlay-gradient":""}},"ast-content-background-meta":{"desktop":{"background-color":"var(--ast-global-color-4)","background-image":"","background-repeat":"repeat","background-position":"center center","background-size":"auto","background-attachment":"scroll","background-type":"","background-media":"","overlay-type":"","overlay-color":"","overlay-opacity":"","overlay-gradient":""},"tablet":{"background-color":"var(--ast-global-color-4)","background-image":"","background-repeat":"repeat","background-position":"center center","background-size":"auto","background-attachment":"scroll","background-type":"","background-media":"","overlay-type":"","overlay-color":"","overlay-opacity":"","overlay-gradient":""},"mobile":{"background-color":"var(--ast-global-color-4)","background-image":"","background-repeat":"repeat","background-position":"center center","background-size":"auto","background-attachment":"scroll","background-type":"","background-media":"","overlay-type":"","overlay-color":"","overlay-opacity":"","overlay-gradient":""}},"footnotes":""},"categories":[1],"tags":[],"class_list":["post-2229","post","type-post","status-publish","format-standard","hentry","category-uncategorized"],"uagb_featured_image_src":{"full":false,"thumbnail":false,"medium":false,"medium_large":false,"large":false,"1536x1536":false,"2048x2048":false,"trp-custom-language-flag":false},"uagb_author_info":{"display_name":"Azar Pamir","author_link":"https:\/\/supplierally.com\/es\/author\/admin\/"},"uagb_comment_info":0,"uagb_excerpt":"Require China supplier serial number allocation records to control issued, applied, packed, held, voided, and reconciled unit identifiers before handover.","_links":{"self":[{"href":"https:\/\/supplierally.com\/es\/wp-json\/wp\/v2\/posts\/2229","targetHints":{"allow":["GET"]}}],"collection":[{"href":"https:\/\/supplierally.com\/es\/wp-json\/wp\/v2\/posts"}],"about":[{"href":"https:\/\/supplierally.com\/es\/wp-json\/wp\/v2\/types\/post"}],"author":[{"embeddable":true,"href":"https:\/\/supplierally.com\/es\/wp-json\/wp\/v2\/users\/1"}],"replies":[{"embeddable":true,"href":"https:\/\/supplierally.com\/es\/wp-json\/wp\/v2\/comments?post=2229"}],"version-history":[{"count":0,"href":"https:\/\/supplierally.com\/es\/wp-json\/wp\/v2\/posts\/2229\/revisions"}],"wp:attachment":[{"href":"https:\/\/supplierally.com\/es\/wp-json\/wp\/v2\/media?parent=2229"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"https:\/\/supplierally.com\/es\/wp-json\/wp\/v2\/categories?post=2229"},{"taxonomy":"post_tag","embeddable":true,"href":"https:\/\/supplierally.com\/es\/wp-json\/wp\/v2\/tags?post=2229"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}