← Back to catalogue

Anti-Cd2

FDA UDI

Class I (US FDA UDI)

by Biogenex Laboratories, Inc.

Identity

Trade Name
ANTI-CD2 FDA UDI
Generic Name
CD2 T-cell marker IVD, antibody FDA UDI
Model / Reference
AM438-5M FDA UDI

Identifiers

Catalog Number
AM438-5M FDA UDI
Primary DI / UDI-DI
00810119670793 FDA UDI
FDA Product Code
NJT FDA UDI
GMDN Term
CD2 T-cell 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

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: CD2 T-cell marker IVD, antibody

Anti-Cd2 by Biogenex Laboratories, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as CD2 T-cell marker IVD, antibody.

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 3b4d3c4c-56df-47db-99dc-dfa2a7264d61 36 fields · synced Jun 8, 2026