Flexible Ureterorenoscopes
by Shanghai Anqing Medical Instrument Co., Ltd 8 variants
Ref US23L-10-USModel US31D-12-US, US31D-12-EU and etc.
Expiring
CE MDR
Valid until
1 Feb 2027
FDA recalls
Not applicable
Documents
Trust
Unverified
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| European Union | CE/MDR | Number6106771CE01 | Date1 May 2026 | StatusExpiring |
Certificates
- 6106771CE01 Expiring
Quality management system EU MDR
- Certifier
- DEKRA Certification B.V. 0344
- Issued
- 1 May 2026
- Expires
- 1 Feb 2027
- Reason
- Mnf data change
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
European Union — CE/MDR Expiring
Specification
- Device Name
- Flexible Ureterorenoscopes
- Model / Reference
- US31D-12-US, US31D-12-EU and etc., US23L-10-US
- Primary DI / UDI-DI
- 06970034211984
- Basic UDI-DI
- 697003421USWW
- EMDN Code
- Z12020713 Ureterorenoscopes
- Device Class
- Class IIa
- EU market of registration
- Italy
Manufacturer details
- EUDAMED SRN
- CN-MF-000008487
- Authorised representative
- Emergo Europe B.V. NL-AR-000000116
Other devices from Shanghai AnQing Medical Instrument Co., Ltd
See all devices from Shanghai AnQing Medical Instrument Co., Ltd →
Properties
Other properties (12)
- 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