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Vimac Video Laryngoscope VM1101

by Hebei Vimed Medical Device Company, Ltd.

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 Number06971834830016 UDI-DI Date30 Sep 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  • Withdrawn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
Vimac Video Laryngoscope
Generic Name
Video intubation laryngoscope handle/monitor
Model / Reference
VM1101
Primary DI / UDI-DI
06971834830016
FDA Product Code
CCW
GMDN Term
Video intubation laryngoscope handle/monitor
Device Class
Class I
Regulation Number
868.5540
GUDID distribution status
In Commercial Distribution

Other devices from Hebei Vimed Medical Device Company, Ltd.

See all devices from Hebei Vimed Medical Device Company, Ltd. →

Properties

  • Premarket Exempt
  • Serial Number
  • Expiration 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
  • Manufacturing Date: No