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Video Laryngoscope VL Pro, VL, VL SE

by Shenzhen Zhixin Biomedical Technology Co., 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 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number06974525071507 UDI-DI Date4 Feb 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  • Withdrawn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
Video Laryngoscope
Generic Name
Video intubation laryngoscope kit
Model / Reference
VL Pro, VL, VL SE
Primary DI / UDI-DI
06974525071507
FDA Product Code
CCW
GMDN Term
Video intubation laryngoscope kit
Device Class
Class I
Regulation Number
868.5540
GUDID distribution status
In Commercial Distribution

Other devices from Shenzhen Zhixin Biomedical Technology Co., Ltd.

Properties

  • Prescription Use
  • Premarket Exempt
  • Serial Number
  • Manufacturing Date

Other properties (10)

  • 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