Surelift Anchorsure
by Desarrollo E Investigacion Medica Aragonesa S.L. 4 variants
Ref CPS01V-ANCHOR
Active
CE MDR
Valid until
19 Mar 2029
FDA recalls
Not applicable
Documents
Trust
Unverified
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| European Union | CE/MDR | Number843656835ANCHORSURENW 08437007606720 | Date18 Sep 2026 | StatusActive |
Certificates
- IZ 1789390-4 Active
Technical documentation EU MDR
- Certifier
- TÜV Rheinland LGA Products GmbH 0197
- Issued
- 20 Mar 2024
- Expires
- 19 Mar 2029
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
European Union — CE/MDR Active
Specification
- Device Name
- Surelift Anchorsure
- Model / Reference
- CPS01V-ANCHOR
- Primary DI / UDI-DI
- 08437007606720
- Basic UDI-DI
- 843656835ANCHORSURENW
- EMDN Code
- P0899 Urogenital prostheses - other
- Device Class
- Class IIb
- EU market of registration
- Germany
Manufacturer details
- EUDAMED SRN
- ES-MF-000004008
Other devices from Desarrollo E Investigacion Medica Aragonesa SL
See all devices from Desarrollo E Investigacion Medica Aragonesa SL →
Properties
Other properties (12)
- Reusable: No
- Contains Latex: No
- Reprocessed: No
- Sutures: 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