DexPure 801-30 8-M
Ref 45 801-30 8-M
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 | Number36038345800121308C 03603835705408 | Date1 Nov 2022 | 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- Withdrawn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
- Dexpure 45801-30
- Model / Reference
- 45 801-30 8-M
- Primary DI / UDI-DI
- 03603835705408
- Basic UDI-DI
- 36038345800121308C
- Direct Marketing DI
- 03603835705408
- EMDN Code
- T010201 Latex examination / treatment gloves
- Device Class
- Class I
- EU market of registration
- France
Manufacturer details
- EUDAMED SRN
- FR-MF-000023170
Other devices from PIP Global Safety France
Properties
Other properties (12)
- Sterile: No
- Implantable: No
- Reusable: 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