Combined spinal and epidural anesthesia kit
by Zhejiang Runqiang Medical Instruments Co., Ltd 2 variants
Ref ASⅡ15125110152311101N7Model AS-E/SII
Active
CE MDR
Valid until
26 Mar 2030
FDA recalls
Not applicable
Documents
Trust
Unverified
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| European Union | CE/MDR | Number697374067003LK 06937401204178 | Date10 Jul 2025 | StatusActive |
Certificates
- G70 082107 0019 Active
Technical documentation EU MDR
- Certifier
- TÜV SÜD Product Service GmbH 0123
- Issued
- 27 Mar 2025
- Expires
- 26 Mar 2030
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
European Union — CE/MDR Active
Specification
- Device Name
- Disposable Anaesthesia Needle and Anaesthesia Kit
- Model / Reference
- AS-E/SII, ASⅡ15125110152311101N7
- Primary DI / UDI-DI
- 06937401204178
- Basic UDI-DI
- 697374067003LK
- Direct Marketing DI
- 06937401204178
- EMDN Code
- A01030103 Combined epidural and spinal anaesthesia needles and kits
- Device Class
- Class III
- EU market of registration
- Germany
Manufacturer details
- EUDAMED SRN
- CN-MF-000005693
- Authorised representative
- Shanghai International Holding Corp. GmbH(Europe) DE-AR-000000001
Other devices from Zhejiang Runqiang Medical Instruments Co., Ltd
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Properties
Other properties (10)
- Implantable: No
- Reusable: No
- Contains Latex: No
- Reprocessed: No
- Human-derived: No
- Human Tissues: No
- Animal Tissues: No
- Administering Medicine: No
- Measuring Function: No
- Incorporates Medicinal Product: No