Artefit
by Sanko Tekstil Isletmeleri Sanayi Ve Ti̇caret Anoni̇m Şirketi Isko Subesi
Ref SPCD0001
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 | Number868452375SPCDRR 08684523754033 | Date19 Jun 2026 | 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- Withdrawn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
- Device Name
- Sequential Pneumatic Compression Device
- Model / Reference
- SPCD0001
- Primary DI / UDI-DI
- 08684523754033
- Basic UDI-DI
- 868452375SPCDRR
- Direct Marketing DI
- 08684523754033
- EMDN Code
- Z120607 Pneumatic compression equipment
- Device Class
- Class IIa
- 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