A-Clamp A-120R
Part of a family of 9 devices: see the family page
Ref A-120RModel A-110, Tube Occluding Clamp
A-Clamp A-120R is a Class I device made by Dravon Medical Inc, registered in EUDAMED on 2 Jul 2026 (Basic UDI-DI 0850048213A110JG) and listed in FDA GUDID since 16 Jan 2023 (UDI-DI 00850048213043), active as of 25 Oct 2026.
Active
CE MDR
Valid until
No date given
FDA recalls
Not checked
Documents
None linked in EUDAMED
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| European Union | CE/MDR EUDAMED | Number0850048213A110JG 00850048213043 | Date2 Jul 2026 | StatusActive |
| United States | GUDID listing GUDID | Number00850048213043 | Date16 Jan 2023 | StatusListed |
Official records
- EUDAMED public site 0850048213A110JG
- AccessGUDID record 00850048213043
Across registries
- EUDAMED Basic UDI-DI 0850048213A110JG registered 2 Jul 2026 Active
- FDA GUDID UDI-DI 00850048213043 listed 16 Jan 2023 Listed
Timeline
- Listed FDA GUDID 00850048213043
- Registered EUDAMED 0850048213A110JG
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
- European Union
- United States
Specification
- Trade name
- A-Clamp, Red (Qty:100) EUDAMEDA-Clamp GUDID
- Generic name
- Medical tubing clip/clamp, temporary, non-calibrated, single-use
- Model / reference
- A-120R, A-110, Tube Occluding Clamp
- Primary DI / UDI-DI
- 00850048213043
- Basic UDI-DI
- 0850048213A110JG
- FDA product code
- HXD
- EMDN code
- Z120499 General medicine instruments - other
- GMDN term
- Medical tubing clip/clamp, temporary, non-calibrated, single-use
- Device class
- Class I
- Regulation number
- 878.4800
- EU registration type
- Standard device
- EU market of registration
- Netherlands
- GUDID distribution status
- In Commercial Distribution
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