Vanocathe Safety
by iLife Medical Devices Pvt Ltd 8 variants
Ref 901.48.06.04Model Intravenous Cannula/Catheter (with/ without safety feature)
Active
CE MDR
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 | Number890603910901FP 08906039102314 | Date7 Nov 2025 | StatusActive |
Certificates
EUDAMED lists no certificate for this device's Basic UDI-DI.
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
European Union — CE/MDR Active
Specification
- Model / Reference
- Intravenous Cannula/Catheter (with/ without safety feature), 901.48.06.04
- Primary DI / UDI-DI
- 08906039102314
- Basic UDI-DI
- 890603910901FP
- EMDN Code
- C0101010201 Peripheral i.v. catheters, with safety systems, with injection valves
- Device Class
- Class IIa
- EU market of registration
- Austria
Manufacturer details
- EUDAMED SRN
- IN-MF-000014372
- Authorised representative
- CMC Medical Devices & Drugs SL ES-AR-000000293
Other devices from iLife Medical Devices Pvt Ltd
Properties
Other properties (12)
- 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