Bioteq
by Bioteque Corporation 1,000+ variants
Part of a family of 2,500+ devices: see the family page
Ref BT-PD4-1630
Bioteq (BT-PD4-1630) is a Class IIa device made by Bioteque Corp., registered in EUDAMED on 7 Oct 2026 (Basic UDI-DI 471988271PDZG), active as of 7 Nov 2026.
Active
CE MDR
Valid until
No date given
FDA recalls
Not applicable
Documents
None linked in EUDAMED
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| European Union | CE/MDR | Number471988271PDZG 04713909214176 | Date7 Oct 2026 | StatusActive |
Official records
- EUDAMED public site 471988271PDZG
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
European Union — CE/MDR Active
Specification
- Device name
- Drainage Catheter Set
- Model / reference
- BT-PD4-1630
- Primary DI / UDI-DI
- 04713909214176
- Basic UDI-DI
- 471988271PDZG
- EMDN code
- A060299 Percutaneous drainage systems - other
- Device class
- Class IIa
- EU registration type
- Standard device
- EU market of registration
- Denmark
Manufacturer details
- EUDAMED SRN
- TW-MF-000015568
- Authorised representative
- MedNet EC-REP GmbH DE-AR-000000002
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