Mooeli iScan Ultra
by Hangzhou ChohoTech Co., Ltd
Model Mooeli iScan Ultra-S、Mooeli iScan Ultra-M、Mooeli iScan Ultra-L、Mooeli iScan Ultra-SP、Mooeli iScan Ultra-MP、Mooeli iScan Ultra-LP、Mooeli iScan Ultra-AP
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 | Number697577604iScanUltraMH 06975776040021 | Date1 Feb 2023 | 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- Withdrawn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
- Mooeli iScan Ultra
- Model / Reference
- Mooeli iScan Ultra-S、Mooeli iScan Ultra-M、Mooeli iScan Ultra-L、Mooeli iScan Ultra-SP、Mooeli iScan Ultra-MP、Mooeli iScan Ultra-LP、Mooeli iScan Ultra-AP
- Primary DI / UDI-DI
- 06975776040021
- Basic UDI-DI
- 697577604iScanUltraMH
- EMDN Code
- V9099 Various devices not included in other classes - other
- Device Class
- Class I
- EU market of registration
- France
Manufacturer details
- EUDAMED SRN
- CN-MF-000029868
- Authorised representative
- SUNGO Europe B.V. NL-AR-000000247
Other devices from Hangzhou ChohoTech Co., Ltd
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