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Ambu® SureSight® Mobile Kit 390471000

by Ambu A/S

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 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number05707480163267 UDI-DI Date19 Dec 2025ListedStatusListed 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  • Withdrawn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
Ambu® SureSight® Mobile Kit
Generic Name
Video intubation laryngoscope handle/monitor
Model / Ref / Catalog
390471000
Primary DI / UDI-DI
05707480163267
FDA Product Code
OGH
GMDN Term
Video intubation laryngoscope handle/monitor
Device Class
Class I
Regulation Number
868.5540
GUDID distribution status
In Commercial Distribution

Other devices from Ambu A/S

See all devices from Ambu A/S →

Properties

  • Prescription Use
  • Convenience Kit
  • Premarket Exempt
  • Lot / Batch Number
  • Serial Number
  • Manufacturing Date

Other properties (8)

  • Sterile: No
  • Single Use: No
  • Implantable: No
  • Contains Latex: No
  • Over-the-Counter: No
  • Combination Product: No
  • HCT/P: No
  • Expiration Date: No