LimFlow V-Ceiver
Ref VC-CE-23Model VC-CE-21
LimFlow V-Ceiver (VC-CE-23) is a Class IIa device made by LimFlow SA, registered in EUDAMED on 27 Oct 2023 (Basic UDI-DI 0850017630VCCE21RS) with CE/MDR certificate 1000261596 valid until 26 Oct 2028, active as of 24 Oct 2026.
Active
CE MDR
Valid until
26 Oct 2028
FDA recalls
Not applicable
Documents
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| European Union | CE/MDR | Number1000261596 | Date21 Aug 2025 | StatusActive |
Official records
- EUDAMED public site 0850017630VCCE21RS
Certificates
- 1000261596 Active
Quality management system EU MDR
- Certifier
- DQS Medizinprodukte GmbH 0297
- Issued
- 21 Aug 2025
- Expires
- 26 Oct 2028
Timeline
- Registered EUDAMED 0850017630VCCE21RS
- Certificate issued EUDAMED 1000261596
- Certificate expires EUDAMED 1000261596
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
European Union — CE/MDR Active
Specification
- Model / reference
- VC-CE-21, VC-CE-23
- Primary DI / UDI-DI
- 00850017630451
- Basic UDI-DI
- 0850017630VCCE21RS
- EMDN code
- C010102 Peripheral i.v. catheter systems
- Device class
- Class IIa
- EU registration type
- Standard device
- EU market of registration
- Germany
Manufacturer details
- EUDAMED SRN
- FR-MF-000011529
Similar devices in this category
Other devices filed under PERIPHERAL I.V. CATHETERS AND CANNULAS.