Anesthesia System
by Medcaptain Medical Technology Co., Ltd. 5 variants
Ref /Model Supaera 50A, Supaera 50, Supaera 50 Plus, Supaera 50 Pro, Supaera 50P
Active
CE MDR
Valid until
Not listed
FDA recalls
Not applicable
Documents
None linked in EUDAMED
Trust
Unverified
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| European Union | CE/MDR | Number69268026Supaera5000000162 06926802613368 | Date13 Aug 2026 | StatusActive |
Certificates
EUDAMED lists no certificate for this device's Basic UDI-DI.
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
European Union — CE/MDR Active
Specification
- Model / Reference
- Supaera 50A, Supaera 50, Supaera 50 Plus, Supaera 50 Pro, Supaera 50P, /
- Primary DI / UDI-DI
- 06926802613368
- Basic UDI-DI
- 69268026Supaera5000000162
- EMDN Code
- Z1203010101 Anaesthesia devices
- Device Class
- Class IIb
- EU market of registration
- Netherlands
Manufacturer details
- EUDAMED SRN
- CN-MF-000005925
- Authorised representative
- Shanghai International Holding Corp. GmbH(Europe) DE-AR-000000001
Other devices from Medcaptain Medical Technology Co., Ltd.
See all devices from Medcaptain Medical Technology Co., Ltd. →
Properties
Other properties (11)
- 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
- Incorporates Medicinal Product: No