Conmed 000615
Ref 000615
Conmed 000615 is a Class I device made by Conmed Corporation, registered in EUDAMED on 11 Nov 2025 (Basic UDI-DI 084585408530D6) and listed in FDA GUDID since 24 Sep 2020 (UDI-DI 10653405050315), active as of 23 Oct 2026.
Active
CE MDR
Valid until
No date given
FDA recalls
Not checked
Documents
None, self-declared
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| European Union | CE/MDR EUDAMED | Number084585408530D6 10653405050315 | Date11 Nov 2025 | StatusActive |
| United States | GUDID listing GUDID | Number10653405050315 | Date24 Sep 2020 | StatusListed |
Official records
- EUDAMED public site 084585408530D6
- AccessGUDID record 10653405050315
Across registries
- EUDAMED Basic UDI-DI 084585408530D6 registered 11 Nov 2025 Active
- FDA GUDID UDI-DI 10653405050315 listed 24 Sep 2020 Listed
Certificates
No certifier certificate is listed. Devices of this class are self-declared by the manufacturer.
Timeline
- Listed FDA GUDID 10653405050315
- Registered EUDAMED 084585408530D6
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
- European Union
- United States
Specification
- Trade name
- Conmed
- Generic name
- Surgical instrument/endoscope cleaning utensil, single-use
- Device name
- Non-orthopedic, Non-active, Accessory, Endoscope Cleaning
- Model / Ref / Catalog
- 000615
- Primary DI / UDI-DI
- 10653405050315
- Basic UDI-DI
- 084585408530D6
- Unit of use DI
- 00653405050318
- FDA product code
- MNL
- EMDN code
- V070101 Endoscopes cleaning brushes - for generic use
- GMDN term
- Surgical instrument/endoscope cleaning utensil, single-use
- Device class
- Class I
- Regulation number
- 876.1500
- EU registration type
- Standard device
- EU market of registration
- Belgium
- GUDID distribution status
- In Commercial Distribution
- Size
- Length — 230 CentimeterOuter Diameter — 2 Millimeter
Similar devices in this category
Other devices filed under CLEANING BRUSHES.