Tunneling KIT CH8
by Raumedic AG
Ref 090516-001
Active
CE MDD
Valid until
Not listed
FDA recalls
Not checked
Documents
None linked in EUDAMED
Trust
Unverified
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| European Union | CE/MDD EUDAMED | NumberB-04057834023541 04057834023541 | Date30 Sep 2026 | StatusActive |
| United States | GUDID listing GUDID | Number04057834023541 | Date8 Dec 2025 | StatusListed |
Certificates
EUDAMED lists no certificate for this device's Basic UDI-DI.
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
- European Union
- United States
Specification
- Generic Name
- Subcutaneous tunneller, single-use
- Model / Reference
- 090516-001
- Primary DI / UDI-DI
- 04057834023541
- Basic UDI-DI
- B-04057834023541
- FDA Product Code
- GWM
- EMDN Code
- Z12109085 Various neurology and neurosurgery instruments - specific materials
- GMDN Term
- Subcutaneous tunneller, single-use
- Device Class
- Class IIa EUDAMEDClass II GUDID
- Regulation Number
- 882.1620
- EU market of registration
- Germany
- GUDID distribution status
- In Commercial Distribution
Truth per registry
| Field | EUDAMED | GUDID |
|---|---|---|
| Device Class | Class IIa | Class II |
Manufacturer details
- EUDAMED SRN
- DE-MF-000006155
Other devices from Raumedic AG
Properties
Other properties (16)
- Implantable: No
- Reusable: No
- Contains Latex: No
- Reprocessed: No
- Human-derived: No
- Human Tissues: No
- Animal Tissues: No
- Administering Medicine: No
- Measuring Function: No
- Incorporates Medicinal Product: No
- Over-the-Counter: No
- Convenience Kit: No
- Combination Product: No
- HCT/P: No
- Premarket Exempt: No
- Serial Number: No