Kanüle
by WILDmedical GmbH 2 variants
Ref KANÜLEModel Ventrikel Drainage System
Active
CE MDR
Valid until
13 Dec 2028
FDA recalls
Not applicable
Documents
Trust
Unverified
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| European Union | CE/MDR | Number426235778MW0120XBD 04262357788765 | Date11 Apr 2024 | StatusActive |
Certificates
- 1000124355 Active
Quality management system EU MDR
- Certifier
- DQS Medizinprodukte GmbH 0297
- Issued
- 14 Dec 2023
- Expires
- 13 Dec 2028
- 1000139301 Active
Technical documentation EU MDR
- Certifier
- DQS Medizinprodukte GmbH 0297
- Issued
- 14 Dec 2023
- Expires
- 13 Dec 2028
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
European Union — CE/MDR Active
Specification
- Device Name
- Duisburger Nadel
- Model / Reference
- Ventrikel Drainage System, KANÜLE
- Primary DI / UDI-DI
- 04262357788765
- Basic UDI-DI
- 426235778MW0120XBD
- EMDN Code
- A0601010299 Drainage systems with adjustable suction - other
- Device Class
- Class III
- EU market of registration
- Germany
Manufacturer details
- EUDAMED SRN
- DE-MF-000017096
Other devices from WILDmedical GmbH
Properties
Other properties (13)
- Sterile: No
- Implantable: No
- Reusable: No
- Contains Latex: No
- Reprocessed: No
- CMR Substance: No
- Human-derived: No
- Human Tissues: No
- Animal Tissues: No
- Endocrine Disruptor: No
- Administering Medicine: No
- Measuring Function: No
- Incorporates Medicinal Product: No