A-Clamp A-110

by Dravon Medical Inc

Part of a family of 9 devices: see the family page

Ref A-110Model A-110, Tube Occluding Clamp

A-Clamp A-110 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 00850048213012), active as of 22 Oct 2026.

Active European Union. Also listed in GUDID (US).

CE MDR

Valid until

No date given

EUDAMED holds no validity date

FDA recalls

Not checked

No FDA submission to match recalls against

Documents

None linked in EUDAMED

A group certificate may exist

Trust

Source EUDAMED, GUDID, synced 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

Region	Authorization	Number	Date	Status
European Union	CE/MDR EUDAMED	Number0850048213A110JG Basic UDI-DI 00850048213012UDI-DI	Date2 Jul 2026Registered	StatusActive
United States	GUDID listing GUDID	Number00850048213012 UDI-DI	Date16 Jan 2023Listed	StatusListed GUDID: in commercial distribution

Official records

EUDAMED public site Basic UDI-DI 0850048213A110JG — open Devices and search for it
AccessGUDID record UDI-DI 00850048213012

Across registries

2 registries list this device

EUDAMED Basic UDI-DI 0850048213A110JG registered 2 Jul 2026 Active
FDA GUDID UDI-DI 00850048213012 listed 16 Jan 2023 Listed

Timeline

2 dated events

16 Jan 2023 Listed FDA GUDID 00850048213012
2 Jul 2026 Registered EUDAMED 0850048213A110JG

Coverage

2 jurisdictions

Active
Expiring
Withdrawn
Listed
Not covered

European Union CE/MDR Active
United States GUDID listing Listed

Specification

EUDAMED · GUDID

Trade name: A-Clamp
Generic name: Medical tubing clip/clamp, temporary, non-calibrated, single-use
Model / reference: A-110, Tube Occluding Clamp

Primary DI / UDI-DI: 00850048213012
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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See all devices from Dravon Medical Inc →

Properties

Premarket exempt
Lot / batch number
Manufacturing date

Other properties (22, all answered No)