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BriteBlade Pro Fiber Optic Single Use Laryngoscope Phillips Blade Size 4 040-744U

by Flexicare Medical Limited

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 Number05055788711872 UDI-DI Date22 Oct 2020ListedStatusListed 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  • Withdrawn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
BriteBlade Pro Fiber Optic Single Use Laryngoscope Phillips Blade Size 4
Generic Name
Laryngoscope blade, single-use
Model / Reference
040-744U
Primary DI / UDI-DI
05055788711872
FDA Product Code
CCW
GMDN Term
Laryngoscope blade, single-use
Device Class
Class I
Regulation Number
868.5540
GUDID distribution status
In Commercial Distribution

Related devices

Category: Laryngoscope blade, single-use

Other devices from Flexicare Medical Limited

See all devices from Flexicare Medical Limited →

Properties

  • Sterile
  • Single Use
  • Premarket Exempt
  • Lot / Batch Number
  • Expiration Date

Other properties (9)

  • Implantable: No
  • Contains Latex: No
  • Prescription Use: No
  • Over-the-Counter: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No
  • Serial Number: No
  • Manufacturing Date: No