Conmed 0048200
Ref 0048200
Conmed 0048200 is a device classified as Class I in the EU and Class II in the US made by Conmed Corporation, registered in EUDAMED on 26 May 2026 (Basic UDI-DI B-20653405000683) and listed in FDA GUDID since 25 Jul 2024 (UDI-DI 20653405000683), active as of 23 Oct 2026.
Active
CE MDD
Valid until
No date given
FDA recalls
Not checked
Documents
None, self-declared
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| European Union | CE/MDD EUDAMED | NumberB-20653405000683 20653405000683 | Date26 May 2026 | StatusActive |
| United States | GUDID listing GUDID | Number20653405000683 | Date25 Jul 2024 | StatusListed |
Official records
- EUDAMED public site B-20653405000683
- AccessGUDID record 20653405000683
Across registries
- EUDAMED Basic UDI-DI B-20653405000683 registered 26 May 2026 Active
- FDA GUDID UDI-DI 20653405000683 listed 25 Jul 2024 Listed
Certificates
No certifier certificate is listed. Devices of this class are self-declared by the manufacturer.
Timeline
- Listed FDA GUDID 20653405000683
- Registered EUDAMED B-20653405000683
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
- European Union
- United States
Specification
- Trade name
- Conmed
- Generic name
- Suction/irrigation tubing, single-use
- Device name
- Surgical Instruments and Accessories
- Model / Ref / Catalog
- 0048200
- Primary DI / UDI-DI
- 20653405000683
- Basic UDI-DI
- B-20653405000683
- FDA product code
- BYY
- EMDN code
- A0680 Drainage and fluid collection devices - accessories
- GMDN term
- Suction/irrigation tubing, single-use
- Device class
- Class I EUDAMEDClass II GUDID
- Regulation number
- 880.6740
- EU registration type
- Legacy device (under a directive)
- EU market of registration
- Belgium
- GUDID distribution status
- In Commercial Distribution
- Size
- Length — 0.46 MeterLength — 1.5 Feet
Truth per registry
| Field | EUDAMED | GUDID |
|---|---|---|
| Device class | Class I | Class II |
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