Curette/Rasp/Scraper/Tonsillectomy instrument, Kürette/Raspel/Schaber/Tonsillektomie-Instrument
by ELCON Medical Instruments GmbH 601 variants
Ref 220-223
Active
CE MDR
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/MDR | Number404911310401R002001001RM 04049113049014 | Date12 Jun 2026 | StatusActive |
Certificates
EUDAMED lists no certificate for this device's Basic UDI-DI.
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
European Union — CE/MDR Active
Specification
- Device Name
- Curette/Rasp/Scraper/Tonsillectomy instrument, Kürette/Raspel/Schaber/Tonsillektomie-Instrument
- Model / Reference
- 220-223
- Primary DI / UDI-DI
- 04049113049014
- Basic UDI-DI
- 404911310401R002001001RM
- Direct Marketing DI
- 04049113049014
- EMDN Code
- L0499 Abdominal surgery instruments, reusable - other
- Device Class
- Class I
- EU market of registration
- Germany
Manufacturer details
- EUDAMED SRN
- DE-MF-000005908
Other devices from ELCON Medical Instruments 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