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Nephroscope 165 802 630

by SOPRO-COMEG GmbH

Nephroscope 165 802 630 is a Class II device made by SOPRO-COMEG GmbH, cleared under FDA 510(k) K945262 on 26 May 1995 and listed in FDA GUDID since 20 Mar 2018 (UDI-DI 04059082030074), active as of 23 Oct 2026.

Active United States. Also listed in GUDID (US).

510(k)

Valid until

No expiry

510(k) clearance is not time-limited

FDA recalls

None found

in data synced 23 Oct 2026

Documents

510(k) K945262

FDA submission, from GUDID

Trust

Unverified

Source GUDID, synced 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number04059082030074 UDI-DI Date20 Mar 2018ListedStatusListed GUDID: in commercial distribution
United StatesFDA 510(k)SESE from GUDID Substantially Equivalent · Traditional NumberK945262 Date26 May 1995DecidedStatusActive

Official records

Across registries

2 registries list this device

  • FDA 510(k) K945262 decided 26 May 1995 Active
  • FDA GUDID UDI-DI 04059082030074 listed 20 Mar 2018 Listed

Timeline

2 dated events

  1. Cleared FDA 510(k) K945262
  2. Listed FDA GUDID 04059082030074

Coverage

1 jurisdiction

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  • Withdrawn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

United States — FDA 510(k) Active

Specification

GUDID

Trade name
Nephroscope
Generic name
Rigid optical nephroscope
Model / reference
165 802 630
Primary DI / UDI-DI
04059082030074
510(k) Number
FDA product code
FAJ
GMDN term
Rigid optical nephroscope
Device class
Class II
Regulation number
876.1500
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

Similar devices

Other devices filed under FDA product code FAJ (Cystoscope and accessories, flexible/rigid).

Other devices from SOPRO-COMEG GmbH

See all devices from SOPRO-COMEG GmbH →

Properties

  • Sterilise before use
  • Lot / batch number
  • Serial number
  • Manufacturing date
Other properties (11, all answered No)