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Bta Trak

FDA UDI

Class II (US FDA UDI)

by Polymedco Cancer Diagnostic Products Llc

Identity

Trade Name
BTA TRAK FDA UDI
Generic Name
Bladder tumour associated antigen IVD, kit, enzyme immunoassay (EIA) FDA UDI
Device Name
BTA TRAK - USA Labeled FDA UDI
Model / Reference
662150 FDA UDI
Description
BTA TRAK - USA Labeled FDA UDI

Identifiers

Primary DI / UDI-DI
00855574005285 FDA UDI
FDA Product Code
MMW FDA UDI
GMDN Term
Bladder tumour associated antigen IVD, kit, enzyme immunoassay (EIA) FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
866.6010 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

Yes

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Bladder tumour associated antigen IVD, kit, enzyme immunoassay (EIA)

Bta Trak by Polymedco Cancer Diagnostic Products Llc — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Bladder tumour associated antigen IVD, kit, enzyme immunoassay (EIA).

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 87cd8d26-c1cc-42e0-83d5-04751e5a961c 34 fields · synced May 31, 2026