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CAS MediLift/MediBom & M20 04061591000370

by Ondal Medical Systems GmbH

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

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number04061591000370 UDI-DI Date12 Jun 2026ListedStatusListed GUDID: 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  • Withdrawn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
CAS MediLift/MediBom & M20
Generic Name
General utility supply system, ceiling-mounted
Model / Reference
04061591000370
Primary DI / UDI-DI
04061591000370
FDA Product Code
FQO
GMDN Term
General utility supply system, ceiling-mounted
Device Class
Class I
Regulation Number
878.4960
GUDID distribution status
In Commercial Distribution

Other devices from Ondal Medical Systems GmbH

See all devices from Ondal Medical Systems GmbH →

Properties

  • Premarket Exempt
  • Serial Number
  • Manufacturing Date

Other properties (11)

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