Z33193-75
by Foosin Medical Supplies Inc., Ltd.
Ref Z33193-75Model PTFE
Z33193-75 is a device classified as Class IIb and Class III in the EU made by Foosin Medical Supplies, Inc., registered in EUDAMED on 11 Jun 2026 (Basic UDI-DI 69418136NA-suturesIIbZ8H), active as of 7 Nov 2026.
Active
CE MDR CE MDD
Valid until
No date given
FDA recalls
Not applicable
Documents
None linked in EUDAMED
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| European Union | CE/MDD | Number69418136NA-suturesIIbZ8H 06941813683414 | Date11 Jun 2026 | StatusActive |
| European Union | CE/MDR | Number69418136NA-suturesIIbZ8H 06941813683414 | Date11 Jun 2026 | StatusActive |
Official records
- EUDAMED public site 69418136NA-suturesIIbZ8H
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
European Union — CE/MDD, CE/MDR Active
Specification
- Model / reference
- PTFE, Z33193-75
- Primary DI / UDI-DI
- 06941813683414
- Basic UDI-DI
- 69418136NA-suturesIIbZ8H, B-06941813683414
- Direct marketing DI
- 06941813683414
- EMDN code
- H010201010501 Polytetrafluoroethylene (ptfe) monofilament with needle
- Device class
- Class IIbClass III
- EU registration type
- Standard deviceLegacy device (under a directive)
- EU market of registration
- LithuaniaHungary
Manufacturer details
- EUDAMED SRN
- CN-MF-000006957
- Authorised representative
- MedNet EC-REP C III GmbH DE-AR-000011196
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