ARTEFIT 8 Chamber Pro Vest Garments Small Left
by Sanko Tekstil Isletmeleri Sanayi Ve Ti̇caret Anoni̇m Şirketi Isko Subesi
Ref SPCG60001
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 | Number868452375SPCGRX 08684523752923 | Date23 Jun 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- Withdrawn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
- Sequential Pneumatic Compression Garments
- Model / Reference
- SPCG60001
- Primary DI / UDI-DI
- 08684523752923
- Basic UDI-DI
- 868452375SPCGRX
- Direct Marketing DI
- 08684523752923
- EMDN Code
- Z120607 Pneumatic compression equipment
- Device Class
- Class I
- EU market of registration
- Türkiye
Manufacturer details
- EUDAMED SRN
- TR-MF-000050088
Other devices from Sanko Tekstil Isletmeleri Sanayi Ve Ti̇caret Anoni̇m Şirketi Isko Subesi
See all devices from Sanko Tekstil Isletmeleri Sanayi Ve Ti̇caret Anoni̇m Şirketi Isko Subesi →
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