A/Herren-Leibbinde, Drell haut, Rückenschnürung
by Werkmeister GmbH + Co. KG 3 variants
Ref 0130
Active
CE MDR
Valid until
Not listed
FDA recalls
Not applicable
Documents
None, self-declared
Trust
Unverified
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| European Union | CE/MDR | Number4048486231101YC | Date1 Sep 2025 | StatusActive |
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- Withdrawn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
- Rumpfstützorthese
- Model / Reference
- 0130
- Primary DI / UDI-DI
- 04048486001766, 04048486001735, 04048486001810, 04048486001834, 04048486001797, 04048486001773, 04048486001827, 04048486001759
- Basic UDI-DI
- 4048486231101YC
- Direct Marketing DI
- 0404848600176604048486001735040484860018100404848600183404048486001797040484860017730404848600182704048486001759
- EMDN Code
- Y060499 Abdominal orthoses - other
- Device Class
- Class I
- EU market of registration
- Germany
Manufacturer details
- EUDAMED SRN
- DE-MF-000005120
Other devices from Werkmeister GmbH + Co. KG
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