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Na 7230001

by SCHÖLLY FIBEROPTIC GmbH

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 Number04250480106440 UDI-DI Date5 Dec 2016ListedStatusListed GUDID: in commercial distribution

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — GUDID listing Listed

Specification

GUDID

Generic Name
Flexible fibreoptic nasopharyngolaryngoscope
Model / Reference
7230001
Primary DI / UDI-DI
04250480106440
FDA Product Code
EOB
GMDN Term
Flexible fibreoptic nasopharyngolaryngoscope
Device Class
Class II
Regulation Number
874.4760
GUDID distribution status
In Commercial Distribution
MRI Safety
MR Unsafe

Related devices

Category: Flexible fibreoptic nasopharyngolaryngoscope

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See all devices from SCHÖLLY FIBEROPTIC GmbH →

Properties

  • Prescription Use
  • Serial Number
  • Manufacturing Date

Other properties (11)

  • Sterile: No
  • Single Use: No
  • Implantable: No
  • Contains Latex: No
  • Over-the-Counter: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No
  • Premarket Exempt: No
  • Lot / Batch Number: No
  • Expiration Date: No