Venaporta
by Venaporta Tibbi Malzemeler Imalat Ithalat Ihracat Sanayi Ve Ticaret Limited Sirketi 910 variants
Ref Neoport-3/0-10Model 750144
Active
CE MDD
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/MDD | NumberB-08699142750144 08699142750144 | Date12 Sep 2023 | StatusActive |
Certificates
EUDAMED lists no certificate for this device's Basic UDI-DI.
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
European Union — CE/MDD Active
Specification
- Device Name
- NEOPORT 3/0 SÜTURLU KEÇE(PLEJİT) / PLEDGET WİTH SUTURE 10 mm ½ Taper Cutting Çift İğneli
- Model / Reference
- 750144, Neoport-3/0-10
- Primary DI / UDI-DI
- 08699142750144
- Basic UDI-DI
- B-08699142750144
- EMDN Code
- H010201020201 Polyester multifilament with needle for open surgery
- Device Class
- Class III
- EU market of registration
- Türkiye
Manufacturer details
- EUDAMED SRN
- TR-MF-000021260
Other devices from Venaporta Tibbi Malzemeler Imalat Ithalat Ihracat Sanayi Ve Ticaret Limited Sirketi
Properties
Other properties (9)
- Reusable: No
- Contains Latex: No
- Reprocessed: No
- Human-derived: No
- Human Tissues: No
- Animal Tissues: No
- Administering Medicine: No
- Measuring Function: No
- Incorporates Medicinal Product: No