Biopsy Forceps Knipsa
by Joline GmbH & Co. KG Germany EUDAMED
Ref KNIPSA500
EMDN C01901102
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| European Union | CE/MDR | Number50565-61-A3-00 | Date28 Nov 2025 | StatusActive |
Coverage
- Active
- Not covered
European Union — CE/MDR Active
Certificates
- 50565-61-A3-00 Reissued
Technical documentation EU MDR
- Notified body
- Notified body 0124
- Issued
- 28 Nov 2025
- Expires
- 29 Nov 2030
- Valid from
- 30 Nov 2025
- 50565-61-A2 Expired
Technical documentation EU MDR
- Notified body
- Notified body 0124
- Issued
- 14 Dec 2021
- Expires
- 29 Nov 2025
- Reason
- Other
Specification
- Device Name
- Biopsy Forceps Knipsa
- Model / Reference
- KNIPSA500
- Primary DI / UDI-DI
- 04250203913355
- Basic UDI-DI
- 42502039802000054
- EMDN Code
- C01901102 Myocardial biopsy kits
- Device Class
- Class III
- Market of Registration
- Sweden
Manufacturer details
- EUDAMED SRN
- DE-MF-000005494
Other devices from Joline GmbH & Co. KG
Properties & raw data
Show properties, registry sources and raw records
Other properties (12)
- Implantable: No
- Reusable: 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
Sources (1)
- EUDAMED 042bcdba-e27d-4950-b750-00fe926c0080