Guante Látex Con Polvo Sanyc V.1 – T.l
by Sanicen S.A.
Ref 176E
Active
CE MDR
Valid until
Not listed
FDA recalls
Not applicable
Documents
None, self-declared
Trust
Unverified
Overview
The GUANTE LÁTEX CON POLVO SANYC V.1 – T.L medical device, designed for diagnostic purposes and testing in human tissues, is a Class I medical device with a sterile status. It is manufactured by Sanicen S.A. and has undergone thorough clinical trials to ensure its safety and efficacy.
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| European Union | CE/MDR | Number8431026Gloves/L/CP/EXC9 08431026001764 | Date11 Mar 2026 | 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- Withdrawn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
- Guantes De Látex Con Polvo Para Examen
- Model / Reference
- 176E
- Primary DI / UDI-DI
- 08431026001764
- Basic UDI-DI
- 8431026Gloves/L/CP/EXC9
- EMDN Code
- T010201 Latex examination / treatment gloves
- Device Class
- Class I
- EU market of registration
- Spain
Manufacturer details
- EUDAMED SRN
- ES-MF-000000738
Other devices from Sanicen S.A.
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