← Back to catalogue

ATRX Rabbit Polyclonal Antibody

EUDAMEDFDA UDI

Class C (EU MDR)

Ref 485A-14Model 485A-1X series

by Cell Marque Corporation

Identity

Trade Name
ATRX Rabbit Polyclonal Antibody EUDAMEDFDA UDI
Generic Name
Alpha thalassemia/mental retardation syndrome X-linked (ATRX) IVD, antibody FDA UDI
Device Name
ATRX Rabbit Polyclonal Antibody EUDAMED
Model / Reference
485A-1X series EUDAMED
485A-14 EUDAMEDFDA UDI

Identifiers

Primary DI / UDI-DI
04065266499322 EUDAMEDFDA UDI
Basic UDI-DI
008416831485A-1CU EUDAMED
FDA Product Code
NJT FDA UDI
EMDN Code
W01030709 PRIMARY ANTISERA FOR IMMUNOHISTOLOGY EUDAMED
GMDN Term
Alpha thalassemia/mental retardation syndrome X-linked (ATRX) IVD, antibody FDA UDI

Classification

Device Class
Class C EUDAMED
Class I FDA UDI
Regulation Number
864.1860 FDA UDI
Market of Registration
Germany EUDAMED
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

EUDAMEDFDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Human Tissues

No

EUDAMED

Animal Tissues

Yes

EUDAMED

Microbial Substances

No

EUDAMED

Reagent

Yes

EUDAMED

Self Testing

No

EUDAMED

Near-Patient Testing

No

EUDAMED

Professional Testing

Yes

EUDAMED

Companion Diagnostics

No

EUDAMED

Surgical Instrument

No

EUDAMED

New Device

No

EUDAMED

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

ATRX Rabbit Polyclonal Antibody by Cell Marque Corporation — Class C — IVDR, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Active

CE/IVDR

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

EUDAMED SRN
US-MF-000028332
Authorised Representative
Emergo Europe B.V. NL-AR-000000116

Sources (2)

  • EUDAMED 33963fd1-4eeb-4f03-8d81-c7c79c016676 61 fields · synced Jul 14, 2026
  • FDA UDI d07c0141-97cc-4910-993a-fb96e9c36aa4 33 fields · synced May 30, 2026