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Anti-Pten

FDA UDI

Class I (US FDA UDI)

by Biogenex Laboratories, Inc.

Identity

Trade Name
ANTI-PTEN FDA UDI
Generic Name
Phosphatase and tensin homolog (PTEN) protein IVD, antibody FDA UDI
Model / Reference
AMB26-5M FDA UDI

Identifiers

Catalog Number
AMB26-5M FDA UDI
Primary DI / UDI-DI
00810119671936 FDA UDI
FDA Product Code
NJT FDA UDI
GMDN Term
Phosphatase and tensin homolog (PTEN) protein 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

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

Dimensions & Sizes

Size
Total Volume — 6 Milliliter FDA UDI

Category: Phosphatase and tensin homolog (PTEN) protein IVD, antibody

Anti-Pten by Biogenex Laboratories, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Phosphatase and tensin homolog (PTEN) protein IVD, antibody.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Biogenex Laboratories, Inc.

Sources (1)

  • FDA UDI a84f60c7-9e24-48af-8e50-99b384d42ffe 36 fields · synced May 30, 2026