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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
Molecular grade buffered sample diluent IVD FDA UDI
Device Name
Viral Transport Media Dilution Matrix FDA UDI
Model / Reference
VTMNEG FDA UDI
Description
Viral Transport Media Dilution Matrix FDA UDI

Identifiers

Catalog Number
VTMNEG FDA UDI
Primary DI / UDI-DI
00850051429684 FDA UDI
FDA Product Code
OHQ FDA UDI
GMDN Term
Molecular grade buffered sample diluent IVD FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
862.1660 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

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Molecular grade buffered sample diluent 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 Molecular grade buffered sample diluent IVD.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 5bd33af6-f507-4ce2-9d0c-9638d37997b5 36 fields · synced May 31, 2026