Amvex Vacuum Regulator LLP

by Ohio Medical LLC

Listed FDA GUDID listing, no authorization on record

Valid until

Not applicable

Database listing, no authorization

FDA recalls

Not checked

No FDA submission to match recalls against

Documents

None

No authorization documents

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source GUDID, synced 23 Oct 2026. What this means

Regulatory status

as of registry sync 23 Oct 2026

Region	Authorization	Number	Date	Status
United States	GUDID listing	Number00628101502058 UDI-DI	Date24 Sep 2016Listed	StatusListed GUDID: in commercial distribution

Coverage

1 jurisdiction

Active
Expiring
Withdrawn
Listed
Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade Name: Amvex Vacuum Regulator
Generic Name: Vacuum suction regulator/regulation set, general-purpose
Model / Reference: LLP

Primary DI / UDI-DI: 00628101502058
FDA Product Code: KDP
GMDN Term: Vacuum suction regulator/regulation set, general-purpose

Device Class: Class II
Regulation Number: 880.6740
GUDID distribution status: In Commercial Distribution

MRI Safety: MR Conditional

Other devices from Ohio Medical LLC

See all devices from Ohio Medical LLC →

Properties

Prescription Use
Premarket Exempt
Serial Number

Other properties (11)

Sterile: No
Single Use: No
Implantable: No
Contains Latex: No
Over-the-Counter: No
Convenience Kit: No
Combination Product: No
HCT/P: No
Lot / Batch Number: No
Expiration Date: No
Manufacturing Date: No