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Tinto Fibrinogen, Polyclonal, RPab
EUDAMEDFDA UDIClass IVD General (EU MDR)
Ref BSB 3048
by Bio SB Inc
Identity
- Trade Name
- Tinto Fibrinogen, Polyclonal, RPab EUDAMEDTinto Fibrinogen, RPab FDA UDI
- Generic Name
- Fibrinogen (Factor I) assay IVD, antibody FDA UDI
- Device Name
- Tinto Fibrinogen, Polyclonal, RPab EUDAMEDFibrinogen is a purified immunoglobulin fraction of rabbit antiserum that is filter sterilized and diluted in buffer pH 7.5. FDA UDI
- Model / Reference
- BSB 3048 EUDAMEDPredilute, 7 ml FDA UDI
- Description
- Fibrinogen is a purified immunoglobulin fraction of rabbit antiserum that is filter sterilized and diluted in buffer pH 7.5. FDA UDI
Identifiers
- Catalog Number
- BSB 3048 FDA UDI
- Primary DI / UDI-DI
- B502BSB30480 EUDAMEDFDA UDI
- Basic UDI-DI
- B-B502BSB30480 EUDAMED
- FDA Product Code
- NJT FDA UDI
- EMDN Code
- W01030709 PRIMARY ANTISERA FOR IMMUNOHISTOLOGY EUDAMED
- GMDN Term
- Fibrinogen (Factor I) assay IVD, antibody FDA UDI
Classification
- Device Class
- Class IVD General EUDAMEDClass I FDA UDI
- Regulation Number
- 864.1860 FDA UDI
- Market of Registration
- Sweden 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
No
FDA UDI
Manufacturing Date
No
FDA UDI
MR Safe FDA UDI
Tinto Fibrinogen, Polyclonal, RPab by Bio Sb, Inc. — Class IVD General — IVDD, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS
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-B502BSB30480 | Class IVD General | Active |
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class IVD General | Pending data |
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Manufacturer
- Manufacturer
- Bio SB Inc
- EUDAMED SRN
- US-MF-000036462
- Authorised Representative
- QAdvis EAR AB SE-AR-000001599
Sources (2)
- EUDAMED 6d866b70-1bed-4d12-ae89-534bb220bc19 61 fields · synced Jul 16, 2026
- FDA UDI 0992a94e-dc3a-44a2-9590-f17a193a4482 34 fields · synced May 30, 2026