← Back to catalogue
Vibrapost
EUDAMEDFDA UDIClass IIa (EU MDR)
Ref noneModel VPA, VPEModel VPA
by B&L Biotech
Identity
- Trade Name
- VIBRAPOST EUDAMEDFDA UDI
- Generic Name
- Root canal post kit FDA UDI
- Device Name
- VIBRAPOST EUDAMED
- Model / Reference
- VPA, VPE EUDAMEDnone EUDAMEDVPA EUDAMEDFDA UDI
Identifiers
- Primary DI / UDI-DI
- 08800019110286 EUDAMEDFDA UDI
- Basic UDI-DI
- 88000191VPTIPRJ EUDAMEDB-08800019110286 EUDAMED
- FDA Product Code
- JET FDA UDI
- EMDN Code
- Q010199 CONSERVATIVE DENTISTRY AND ENDODONTICS DEVICES - OTHER EUDAMED
- GMDN Term
- Root canal post kit FDA UDI
Classification
- Device Class
- Class IIa EUDAMEDClass I FDA UDI
- Regulation Number
- 872.6650 FDA UDI
- Market of Registration
- Poland EUDAMED
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
EUDAMEDFDA UDI
Single Use
No
FDA UDI
Implantable
No
EUDAMEDFDA UDI
Reusable
No
EUDAMED
Contains Latex
No
EUDAMEDFDA UDI
Reprocessed
No
EUDAMED
CMR Substance
No
EUDAMED
Human-derived
No
EUDAMED
Human Tissues
No
EUDAMED
Animal Tissues
No
EUDAMED
Endocrine Disruptor
No
EUDAMED
Administering Medicine
No
EUDAMED
Measuring Function
No
EUDAMED
Incorporates Medicinal Product
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
Yes
FDA UDI
Moist Heat or Steam Sterilization FDA UDI
Vibrapost by B&L Biotech — Class IIa — MDD, MDR, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS
Authorization Coverage (2 countries)
Regulatory Authorizations
European Union Active
CE/MDD
European Union Active
CE/MDR
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| EUDAMED | European Union | CE/MDD | 88000191VPTIPRJ | Class IIa | Active |
| EUDAMED | European Union | CE/MDR | 88000191VPTIPRJ | Class IIa | Active |
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class IIa | Pending data |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- B&L Biotech
- EUDAMED SRN
- KR-MF-000023296
- Authorised Representative
- Emergo Europe B.V. NL-AR-000000116
Sources (4)
- EUDAMED 520d6541-c060-4956-a72e-dc8936105f20 61 fields · synced Jul 9, 2026
- EUDAMED 44e49430-6d84-4889-a75c-467fe3f55596 61 fields · synced May 18, 2026
- FDA UDI bf7c3549-3a06-4b92-be8e-f611d2cd0784 32 fields · synced May 29, 2026
- EUDAMED 520d6541-c060-4956-a72e-dc8936105f20-1 61 fields · synced Jun 11, 2026