← Back to catalogue
Tinto FOXP3, Polyclonal, RPab
EUDAMEDFDA UDIClass IVD General (EU MDR)
Ref BSB 6758
by Bio SB Inc
Identity
- Trade Name
- Tinto FOXP3, Polyclonal, RPab EUDAMEDTinto FOXP3 RMab FDA UDI
- Generic Name
- Forkhead box protein (FOX) IVD, antibody FDA UDI
- Device Name
- Tinto FOXP3, Polyclonal, RPab EUDAMEDAnti FOXP3 is a purified immunoglobulin fraction of rabbit antiserum that is filter sterilized and diluted in buffer pH 7.5, containing BSA and sodium azide as a preservative. FDA UDI
- Model / Reference
- BSB 6758 EUDAMEDpredilute, 3 ml FDA UDI
- Description
- Anti FOXP3 is a purified immunoglobulin fraction of rabbit antiserum that is filter sterilized and diluted in buffer pH 7.5, containing BSA and sodium azide as a preservative. FDA UDI
Identifiers
- Catalog Number
- BSB 6758 FDA UDI
- Primary DI / UDI-DI
- B502BSB67580 EUDAMEDFDA UDI
- Basic UDI-DI
- B-B502BSB67580 EUDAMED
- FDA Product Code
- NJT FDA UDI
- EMDN Code
- W01030709 PRIMARY ANTISERA FOR IMMUNOHISTOLOGY EUDAMED
- GMDN Term
- Forkhead box protein (FOX) 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
No
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
MR Safe FDA UDI
Tinto FOXP3, 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-B502BSB67580 | Class IVD General | Active |
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class IVD General | Pending data |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Bio SB Inc
- EUDAMED SRN
- US-MF-000036462
- Authorised Representative
- QAdvis EAR AB SE-AR-000001599
Sources (2)
- EUDAMED 0794202d-014b-4172-8fbc-94ee5c82ce89 61 fields · synced Jun 18, 2026
- FDA UDI 1259add0-256a-4e41-8186-c0ac9ee3aa97 34 fields · synced May 30, 2026