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URO-3 Triple Stain (CD44+p53) with CK20

FDA UDI

Class I (US FDA UDI)

by Biocare Medical, Llc

Identity

Trade Name
URO-3 Triple Stain (CD44+p53) with CK20 FDA UDI
Generic Name
Multiple bladder tissue/tumour marker IVD, antibody FDA UDI
Model / Reference
PM370TSAA FDA UDI

Identifiers

Primary DI / UDI-DI
00847627011718 FDA UDI
FDA Product Code
NJT FDA UDI
GMDN Term
Multiple bladder tissue/tumour marker IVD, antibody FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
864.1860 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

Yes

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: Multiple bladder tissue/tumour marker IVD, antibody

URO-3 Triple Stain (CD44+p53) with CK20 by Biocare Medical, Llc — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Multiple bladder tissue/tumour marker IVD, antibody.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Biocare Medical, Llc

Sources (1)

  • FDA UDI 121ab87f-c74a-4811-9e4f-e09458a649a6 33 fields · synced May 31, 2026