Compliance research

Test, Time, Prothrombin (GJS) — recorded UDI portfolio and field relationships

The acquired full AccessGUDID release records 99 published device records linked to FDA product code GJS. Compare their recorded field relationships below when planning a portfolio mapping. The counts describe this dated public corpus, not unique product models, market size, demand, approval or a test requirement for your device.

Evidence retrieved 2026-10-06. Source versions and topic-specific limits are listed below.

Recorded UDI portfolio · exact code GJS

What does this dated public cohort contain?

99Published device records
35Parsed device count above one
0Device count missing or unresolved

These are primary-DI record counts, not unique model counts or market size. A DI can be linked to more than one product code, so code cohorts must not be added as unique devices.

Recorded indicatorTrueFalseBlank/missingUnrecognized
Packaged as sterile30960
Sterilization required before use00990
Single-use indicator330660
Lot/batch indicator870120
Serial-number indicator230760
Manufacturing-date indicator280710
Expiration-date indicator860130

A blank flag is unknown. A true indicator is a recorded label-data fact; it is not a validation report, FDA approval or a test obligation for your product.

Compare the two sterility questions independently

Packaged as sterileSterilization before useRecorded devices
missingmissing96
truemissing3

These distinct questions describe the supplied device and user instructions. Review the exact FDA field relationship; do not infer a manufacturer’s validated process from these flags.

Source, filters, reconciliation and limitations

Join acquired full-release device.txt to distinct productCodes.txt relationships by exact PrimaryDI; filter exact FDA code and Published device-record state. Count each DI once within that code. Interpret only literal true/false; blank and unrecognized values remain separate. Parse a positive integer deviceCount for the greater-than-one indicator. Do not apply saved daily updates.

Excluded/unresolved recorded states: {}. Global source-relationship exclusions: {}.

Recorded identities/flags only. Not unique product models, market size, demand, approval, validated sterility, a compliance rate or a mandatory test plan. One DI can occur in several different code cohorts; overall cohort counts must not be added as unique devices.

Calculation gudid-exact-code-portfolio-1 · snapshot b9e4fee0ed7afdf9c255a6f0d353df3d17abf768423abba82bb80ceb9b79366c. Counts use the full release; downloaded daily updates are not applied. Corpus download: source 2

Prepare the related field workflows

Use the recorded variation to prepare your mapping

Use this checklist to gather your business or product details before speaking with a specialist. The items below explain what to record and suggest useful supporting documents. You can add your own answers in the editable project brief.

  1. Primary-DI package count and unit-of-use relationship

    35 of 99 records have a parsed device count above one. Compare your controlled count to the separate primary/unit-of-use fields; the cohort cannot decide your count.

    Useful evidence: Your label, package drawing, device count and proposed unit-of-use relationship.

  2. Supplied sterility versus sterilization before use

    The two columns are independent. Use the cross-table to identify the recorded variation, then map your own supplied-state and approved user-instruction evidence separately. A true flag is not a validation report.

    Useful evidence: Approved packaging/labels, IFU and a separate validation-evidence question if statements are unresolved.

  3. Production-identifier indicators

    Compare the recorded lot/batch, serial and date indicators below with your barcode design. These are flags, not actual lot/serial/date values; missing source flags remain unknown.

    Useful evidence: Approved barcode/identifier specification with the DI-level flags separated from unit and batch data.

  4. Resolve differences before uploading

    Document your field/relationship decisions and differences from these public examples; a published record does not certify that its choices fit your product. Ask the specialist to reconcile the controlled evidence and current instructions.

    Useful evidence: A field mapping, conditional-input list and controlled source-to-target reconciliation.

Work packages and dependencies

Questions for providers

Sources and data dates

Read the official document in context. The audit details identify the precise locators and preserved versions used for this page.

FDA openFDA — device classification records ↗

2026-10-05 · retrieved 2026-10-06

Audit details: precise locators and snapshot identifiers

Source key D01 · snapshot 936de5f5d47b9293b702fc32512a79173969fb788c74a63d9b91abe73f3b86a5

  • [1] device-classification-0001-of-0001.json:results[5175] · record eca17fc384f20549e9f4838d398a7b466214c75c79b7655a08a0c32ba96819c9

Prepare an editable project brief

Confirm the facts, scope and contact preference before sharing your project. Preparing this page sends no provider outreach.

Choose work packages to discuss

Compare FDA GUDID Submission Tools