Probe
Ref M13-005-25, M13-005-14
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 | Number++G410M1300525RB | Date5 Jun 2023 | 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- Withdrawn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
- M13-005-25, M13-005-14
- Primary DI / UDI-DI
- G410M13005250, G410M13005140
- Basic UDI-DI
- ++G410M1300525RB, ++G410M1300514R6
- EMDN Code
- L031102 Exploration probes, reusable
- Device Class
- Class I
- EU market of registration
- Romania
Manufacturer details
- EUDAMED SRN
- PK-MF-000031501
- Authorised representative
- ANTEX MEDI SOLUTION DE-AR-000008078
Other devices from Mehrish Industries Pvt Ltd
Properties
Other properties (12)
- Sterile: No
- Implantable: 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