Skip to content

Ohio Medical Vacuum Regulator LISA

by Ohio Medical LLC 2 variants

Listed FDA GUDID listing, not in commercial distribution

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

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number08688250002245 UDI-DI Date24 Sep 2016ListedStatusListed GUDID: not in commercial distribution

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade Name
Ohio Medical Vacuum Regulator
Generic Name
Vacuum suction regulator/regulation set, general-purpose
Model / Reference
LISA
Primary DI / UDI-DI
08688250002245
FDA Product Code
KDP
GMDN Term
Vacuum suction regulator/regulation set, general-purpose
Device Class
Class II
Regulation Number
880.6740
GUDID distribution status
Not 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