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VALIDATE® FIBRINOGEN Test Set
EUDAMEDFDA UDIClass IVD General (EU MDR)
Ref 904st
Identity
- Trade Name
- VALIDATE® FIBRINOGEN Test Set EUDAMEDValidate FDA UDI
- Generic Name
- Fibrinogen assay (factor I) IVD, control FDA UDI
- Device Name
- VALIDATE® FIBRINOGEN Test Set EUDAMEDValidate Fibrinogen is intended for the quantitative determination of Calibration Verification/Linearity of fibrinogen on automated instruments. FDA UDI
- Model / Reference
- 904st EUDAMEDFDA UDI
- Description
- Validate Fibrinogen is intended for the quantitative determination of Calibration Verification/Linearity of fibrinogen on automated instruments. FDA UDI
Identifiers
- Catalog Number
- 904st FDA UDI
- Primary DI / UDI-DI
- 00859110005135 EUDAMEDFDA UDI
- Basic UDI-DI
- B-00859110005135 EUDAMED
- FDA Product Code
- GIL FDA UDI
- EMDN Code
- W0103020799 HAEMOSTASIS CONTROLS - OTHER EUDAMED
- GMDN Term
- Fibrinogen assay (factor I) IVD, control FDA UDI
Classification
- Device Class
- Class IVD General EUDAMEDClass II FDA UDI
- Regulation Number
- 864.7340 FDA UDI
- Market of Registration
- Ireland EUDAMED
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
EUDAMEDFDA UDI
Single Use
Yes
FDA UDI
Implantable
No
FDA UDI
Contains Latex
No
FDA UDI
Human Tissues
Yes
EUDAMED
Animal Tissues
Yes
EUDAMED
Microbial Substances
No
EUDAMED
Reagent
No
EUDAMED
Self Testing
No
EUDAMED
Near-Patient Testing
No
EUDAMED
Professional Testing
Yes
EUDAMED
Companion Diagnostics
No
EUDAMED
Surgical Instrument
No
EUDAMED
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
VALIDATE® FIBRINOGEN Test Set by LGC Clinical Diagnostics, Inc. — Class IVD General — IVDD, FDA UDI — listed in EUDAMED, FDA GUDID
Authorization Coverage (2 countries)
Regulatory Authorizations
European Union Active
CE/IVDD
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| EUDAMED | European Union | CE/IVDD | B-00859110005135 | Class IVD General | Active |
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class IVD General | Pending data |
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Manufacturer
- Manufacturer
- LGC Clinical Diagnostics, Inc.
- EUDAMED SRN
- US-MF-000029697
- Authorised Representative
- MediMark Europe Sarl. FR-AR-000000182
Sources (2)
- EUDAMED d270280b-fb6a-46d9-b1bb-3e4b35bfe62c 61 fields · synced Jun 17, 2026
- FDA UDI 52311f6a-f267-4705-b8a1-ae2f4378f1db 37 fields · synced May 29, 2026