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NA 21.0051a

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 Number04250480101568 UDI-DI Date4 Jan 2018ListedStatusListed 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  • Withdrawn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
Rigid optical arthroscope, reusable
Model / Reference
21.0051a
Primary DI / UDI-DI
04250480101568
FDA Product Code
HRX
GMDN Term
Rigid optical arthroscope, reusable
Device Class
Class II
Regulation Number
888.1100
GUDID distribution status
In Commercial Distribution
MRI Safety
MR Unsafe

Related devices

Category: Rigid optical arthroscope, reusable

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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