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Tipcam 28164FA3D

by Karl Storz SE & CO. KG

Tipcam 28164FA3D is a Class II device made by Karl Storz SE & CO. KG, listed in FDA GUDID since 2 Mar 2020 (UDI-DI 04048551416174), registry data as of 22 Oct 2026.

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

Source GUDID, synced 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number04048551416174 UDI-DI Date2 Mar 2020ListedStatusListed GUDID: in commercial distribution

Official records

Coverage

1 jurisdiction

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  • Withdrawn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

United States — GUDID listing Listed

Specification

GUDID

Trade name
Tipcam
Generic name
Rigid optical intracranial/spinal endoscope, reusable
Model / reference
28164FA3D
Primary DI / UDI-DI
04048551416174
FDA product code
GWG
GMDN term
Rigid optical intracranial/spinal endoscope, reusable
Device class
Class II
Regulation number
882.1480
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

Similar devices

Other devices filed under FDA product code GWG (Endoscope, neurological).

Other devices from Karl Storz SE & CO. KG

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Properties

  • Sterilise before use
  • Prescription use
  • Serial number
Other properties (12, all answered No)