← Back to catalogue

Fort Worth Diagnostics

FDA UDI

Class I (US FDA UDI)

by Fort Worth Diagnostics Llc

Identity

Trade Name
Fort Worth Diagnostics FDA UDI
Generic Name
Assay development analyte-specific reagent IVD FDA UDI
Device Name
Measles Primer Set FDA UDI
Model / Reference
MEAS001 FDA UDI
Description
Measles Primer Set FDA UDI

Identifiers

Catalog Number
MEAS001 FDA UDI
Primary DI / UDI-DI
00850051429530 FDA UDI
FDA Product Code
MVU FDA UDI
GMDN Term
Assay development analyte-specific reagent IVD FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
864.4020 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

No

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

No

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Assay development analyte-specific reagent IVD

Fort Worth Diagnostics by Fort Worth Diagnostics Llc — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Assay development analyte-specific reagent IVD.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Sources (1)

  • FDA UDI b346be74-b291-47f3-9bfc-5597b3d3d804 36 fields · synced Jun 6, 2026