Druckflexible Lagerungssysteme
by Moltoplast GmbH 64 variants
Ref X2009
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 | Number9006018DFLAP 90060180200174 | Date16 Sep 2022 | 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- Withdrawn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
- Druckflexible Lagerungssysteme
- Model / Reference
- X2009
- Primary DI / UDI-DI
- 90060180200174
- Basic UDI-DI
- 9006018DFLAP
- Direct Marketing DI
- 90060180200174
- EMDN Code
- V080399 Medical cushions - other
- Device Class
- Class I
- EU market of registration
- Austria
Manufacturer details
- EUDAMED SRN
- AT-MF-000004503
Other devices from Moltoplast 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