Scherengriff PRO-Linie / 2-teilig
by WISAP Medical Technology GmbH 2 variants
Ref 7301HNR2
Active
CE MDR 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 | Number42505174MISProLine7K 04250517403375 | Date15 Oct 2026 | StatusActive |
| European Union | CE/MDR | Number42505174MISProLine7K 04250517403375 | Date15 Oct 2026 | StatusActive |
Certificates
EUDAMED lists no certificate for this device's Basic UDI-DI.
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
European Union — CE/MDD, CE/MDR Active
Specification
- Trade Name
- Scherengriff PRO-Linie / 2-teiligScherengriff
- Device Name
- Pro-Line Dissecting and Grasping Forceps
- Model / Reference
- 7301HNR2
- Primary DI / UDI-DI
- 04250517403375
- Basic UDI-DI
- 42505174MISProLine7K, B-04250517403375
- EMDN Code
- L1213 Laparoscopic and thoracoscopic surgery handpieces, reusable
- Device Class
- Class IIa
- EU market of registration
- Germany
Manufacturer details
- EUDAMED SRN
- DE-MF-000009935
Other devices from WISAP Medical Technology GmbH
Properties
Other properties (12)
- Sterile: No
- Implantable: 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