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Pashley Laryngoscope 1412-568

by Sontec Instruments, Inc.

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 Number00192896122192 UDI-DI Date30 Oct 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  • Withdrawn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
Pashley Laryngoscope
Generic name
Rigid bladed intubation laryngoscope, optical, reusable
Model / Ref / Catalog
1412-568
Primary DI / UDI-DI
00192896122192
FDA product code
CCW
GMDN term
Rigid bladed intubation laryngoscope, optical, reusable
Device class
Class I
Regulation number
868.5540
GUDID distribution status
In Commercial Distribution
Sterilisation method
Dry Heat Sterilization
Size
Lumen/Inner Diameter — 6 Millimeter

Other devices from Sontec Instruments, Inc.

See all devices from Sontec Instruments, Inc. →

Properties

  • Sterilise before use
  • Prescription use
  • Premarket exempt
  • Lot / batch number

Other properties (11)

  • Supplied sterile: No
  • Single use: No
  • Implantable: No
  • Contains latex: No
  • Over-the-counter: No
  • Convenience kit: No
  • Combination product: No
  • HCT/P: No
  • Serial number: No
  • Expiration date: No
  • Manufacturing date: No