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This is to test the length of the brand field and what it looks like in the GUDI

FDA UDI

Class I (US FDA UDI)

by Life Technologies Limited

Identity

Trade Name
This is to test the length of the brand field and what it looks like in the GUDI FDA UDI
Generic Name
Reverse transcription reagent kit IVD FDA UDI
Device Name
Test Device Description FDA UDI
Model / Reference
A11474 FDA UDI
Description
Test Device Description FDA UDI

Identifiers

Primary DI / UDI-DI
17503025060276 FDA UDI
FDA Product Code
JJH FDA UDI
GMDN Term
Reverse transcription reagent kit IVD FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
862.2310 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Reverse transcription reagent kit IVD

This is to test the length of the brand field and what it looks like in the GUDI by Life Technologies Limited — Class I — FDA UDI — listed in FDA GUDID

Similar devices

Also classified as Reverse transcription reagent kit IVD.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Life Technologies Limited

Sources (1)

  • FDA UDI 5d1c77eb-6208-4207-9efb-12f144d45d80 33 fields · synced Jun 1, 2026