2510 Betai̇pek Tibbi̇ İpek Flaster 10 Cm X 5 M
by Betasan Tibbi̇ Bant San. Ve Ti̇c. A.Ş.
Ref 2510 BETAİPEK TIBBİ İPEK FLASTERModel 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 08683249000356 | 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- Withdrawn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
- Device Name
- 2501 Betai̇pek Tibbi̇ İpek Flaster 1,25 Cm X 5 M
- Model / Reference
- 2501 BETAİPEK TIBBİ İPEK FLASTER, 2510 BETAİPEK TIBBİ İPEK FLASTER
- Primary DI / UDI-DI
- 08683249000356
- 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.
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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