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NA 41.0665a

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 Number04250480106174 UDI-DI Date16 Apr 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  • Withdrawn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

Generic Name
Stone/foreign-body extraction set
Model / Reference
41.0665a
Primary DI / UDI-DI
04250480106174
FDA Product Code
FGA, FEC, FED
GMDN Term
Stone/foreign-body extraction set
Device Class
Class II
Regulation Number
876.1500
GUDID distribution status
In Commercial Distribution
Sterilization Method
Moist Heat or Steam Sterilization
MRI Safety
MR Unsafe

Other devices from SCHÖLLY FIBEROPTIC GmbH

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    Class IIa
  • SmartVue®

    Class I
  • 41.0600d

    Class I
  • 11-0441-A

    Class IIa
  • 95-3985

    Class I
  • 11-0431-B

    Class IIa

See all devices from SCHÖLLY FIBEROPTIC GmbH →

Properties

  • Prescription Use
  • Convenience Kit
  • Serial Number
  • Manufacturing Date

Other properties (10)

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