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Na 825639

by Richard Wolf GmbH

Listed FDA GUDID listing, not in commercial distribution

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 Number04055207009499 UDI-DI Date27 Sep 2016ListedStatusListed GUDID: not 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  • Withdrawn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
Rigid optical oesophagoscope
Model / Ref / Catalog
825639, 8256.39
Description
ESOPHAGOSCOPE-TUBE ID 11.5X7.5MM model Wolf, OD 13.5x9.5mm, TL 494mm, with fixed distal light carrier, graduated, reusable
Primary DI / UDI-DI
04055207009499
FDA Product Code
EOX
GMDN Term
Rigid optical oesophagoscope
Device Class
Class II
Regulation Number
874.4710
GUDID distribution status
Not in Commercial Distribution

Other devices from Richard Wolf GmbH

See all devices from Richard Wolf GmbH →

Properties

  • Premarket Exempt
  • Lot / Batch Number
  • Manufacturing Date

Other properties (11)

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