Quiver
by Nouvag AG
Ref 4044
Quiver (4044) is a Class I device made by Nouvag AG, registered in EUDAMED on 20 Oct 2026 (Basic UDI-DI ++ENOU100036LS), active as of 7 Nov 2026.
Active
CE MDR
Valid until
No date given
FDA recalls
Not applicable
Documents
None, self-declared
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| European Union | CE/MDR | Number++ENOU100036LS +ENOU40441G | Date20 Oct 2026 | StatusActive |
Official records
- EUDAMED public site ++ENOU100036LS
Certificates
No certifier certificate is listed. Devices of this class are self-declared by the manufacturer.
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
European Union — CE/MDR Active
Specification
- Device name
- Liposuction Accessories
- Model / reference
- 4044
- Primary DI / UDI-DI
- +ENOU40441G
- Basic UDI-DI
- ++ENOU100036LS
- EMDN code
- Z12019080 Various instruments for general and multidisciplinary surgery - hardware accessories
- Device class
- Class I
- EU registration type
- Standard device
- EU market of registration
- Germany
Manufacturer details
- EUDAMED SRN
- CH-MF-000018882
- Authorised representative
- Nouvag GmbH DE-AR-000005643
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