2501 Betai̇pek Tibbi̇ İpek Flaster 1, 25 Cm X 5 M
by Betasan Tibbi̇ Bant San. Ve Ti̇c. A.Ş.
Ref 2501 BETAİPEK TIBBİ İPEK FLASTER 1,25 CM X 5 MModel 2501 BETAİPEK TIBBİ İPEK FLASTER
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 | Number8683249FLS2009Y4 08683249000325 | Date12 Oct 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- Withdrawn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
- Model / Reference
- 2501 BETAİPEK TIBBİ İPEK FLASTER, 2501 BETAİPEK TIBBİ İPEK FLASTER 1, 25 CM X 5 M
- Primary DI / UDI-DI
- 08683249000325
- Basic UDI-DI
- 8683249FLS2009Y4
- EMDN Code
- M050101 Plasters on spools (rolls)
- Device Class
- Class I
- EU market of registration
- Türkiye
Manufacturer details
- EUDAMED SRN
- TR-MF-000026740
Other devices from Betasan Tibbi̇ Bant San. Ve Ti̇c. A.Ş.
See all devices from Betasan Tibbi̇ Bant San. Ve Ti̇c. A.Ş. →
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