Asahi KASEI
by Bain Medical Equipment(Guangzhou)Co., Ltd. 22 variants
Ref AVF-D-BR2530BEDS-17Model BAIN-A.V.F-001DE ~BAIN-A.V.F-112DE, BAIN-A.V.F-001ADE ~BAIN-A.V.F-100ADE, BAIN-A.V.F-001VDE ~BAIN-A.V.F-100VDE, BAIN-A.V.F-001DTE ~BAIN-A.V.F-100DTE
Active
CE MDR CE MDD
Valid until
Not listed
FDA recalls
Not applicable
Documents
None linked in EUDAMED
Trust
Unverified
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| European Union | CE/MDR | NumberB-06948082771507 06948082771507 | Date28 May 2026 | StatusActive |
| European Union | CE/MDD | NumberB-06948082771507 06948082771507 | Date28 May 2026 | StatusActive |
Certificates
EUDAMED lists no certificate for this device's Basic UDI-DI.
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
European Union — CE/MDR, CE/MDD Active
Specification
- Trade Name
- Asahi KASEIAsahi KASEI Disposable A.V.Fistula Needle Sets(Dull Needle series )
- Device Name
- Disposable A.V. Fistula Needle Sets(Dull needle series)Disposable A.V. Fistula Needle Sets (Dull Needle series)
- Model / Reference
- AVF-D-BR2530BEDS-17, BAIN-A.V.F-001DE ~BAIN-A.V.F-112DE, BAIN-A.V.F-001ADE ~BAIN-A.V.F-100ADE, BAIN-A.V.F-001VDE ~BAIN-A.V.F-100VDE, BAIN-A.V.F-001DTE ~BAIN-A.V.F-100DTE
- Primary DI / UDI-DI
- 06948082771507
- Basic UDI-DI
- B-06948082771507, 6948082702142A3
- EMDN Code
- A010401 Arteriovenous fistula needles
- Device Class
- Class IIa
- EU market of registration
- Germany
Manufacturer details
- EUDAMED SRN
- CN-MF-000005196
- Authorised representative
- Medical Technology Promedt Consulting GmbH DE-AR-000000085
Other devices from Bain Medical Equipment(Guangzhou)Co., Ltd.
See all devices from Bain Medical Equipment(Guangzhou)Co., Ltd. →
Properties
Other properties (11)
- Implantable: No
- Reusable: No
- Contains Latex: No
- Reprocessed: No
- Human-derived: No
- Human Tissues: No
- Animal Tissues: No
- Endocrine Disruptor: No
- Administering Medicine: No
- Measuring Function: No
- Incorporates Medicinal Product: No