Lastofa
by Ofa Bamberg GmbH 1,000+ variants
Ref 015101082404C0Model Rundstrick
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 | Number4018839K019G 04052727185368 | Date9 Jun 2026 | 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- Withdrawn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
- Rundstrick
- Model / Reference
- Rundstrick, 015101082404C0
- Primary DI / UDI-DI
- 04052727185368
- Basic UDI-DI
- 4018839K019G
- Direct Marketing DI
- 04052727185368
- EMDN Code
- M030405 Compression stockings
- Device Class
- Class I
- Market of Registration
- Germany
Manufacturer details
- EUDAMED SRN
- DE-MF-000008470
Other devices from Ofa Bamberg 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