← Back to catalogue
Glial Fibrillary Acidic Protein (EP672Y) Rabbit Monoclonal Primary Antibody
EUDAMEDFDA UDIClass C (EU MDR)
Ref 258R-17Model 258R-1X series
Identity
- Trade Name
- Glial Fibrillary Acidic Protein (EP672Y) Rabbit Monoclonal Primary Antibody EUDAMEDFDA UDI
- Generic Name
- Glial fibrillary acidic protein (GFAP) IVD, antibody FDA UDI
- Device Name
- Glial Fibrillary Acidic Protein (EP672Y) Rabbit Monoclonal Primary Antibody EUDAMEDFDA UDI
- Model / Reference
- 258R-1X series EUDAMED258R-17 EUDAMEDFDA UDI
- Description
- Glial Fibrillary Acidic Protein (EP672Y) Rabbit Monoclonal Primary Antibody FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00841683120568 EUDAMEDFDA UDI
- Basic UDI-DI
- 008416831258R-1EB EUDAMED
- FDA Product Code
- NJT FDA UDI
- EMDN Code
- W01030709 PRIMARY ANTISERA FOR IMMUNOHISTOLOGY EUDAMED
- GMDN Term
- Glial fibrillary acidic protein (GFAP) IVD, antibody FDA UDI
Classification
- Device Class
- Class C EUDAMEDClass 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
Glial Fibrillary Acidic Protein (EP672Y) Rabbit Monoclonal Primary Antibody by Cell Marque Corporation — Class C — IVDR, FDA UDI — listed in EUDAMED, FDA GUDID
Authorization Coverage (2 countries)
Regulatory Authorizations
European Union Active
CE/IVDR
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| EUDAMED | European Union | CE/IVDR | 008416831258R-1EB | Class C | Active |
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class C | Pending data |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Cell Marque Corporation
- EUDAMED SRN
- US-MF-000028332
- Authorised Representative
- Emergo Europe B.V. NL-AR-000000116
Sources (2)
- EUDAMED 43f8472e-bc16-4ee3-b924-4c4c3324a57c 61 fields · synced Jun 18, 2026
- FDA UDI 367d7b0c-f0be-47fc-bf2f-ff25644a8477 34 fields · synced May 30, 2026