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Unidrive 20711620-1

by Karl Storz SE & CO. KG

Unidrive 20711620-1 is a Class II device made by Karl Storz SE & CO. KG, listed in FDA GUDID since 23 Sep 2016 (UDI-DI 04048551071601), 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 Number04048551071601 UDI-DI Date23 Sep 2016ListedStatusListed 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  • Withdrawn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
Unidrive
Generic name
ENT shaver system
Model / reference
20711620-1
Primary DI / UDI-DI
04048551071601
FDA product code
ERL
GMDN term
ENT shaver system
Device class
Class II
Regulation number
874.4250
GUDID distribution status
In Commercial Distribution

Related devices

Category: ENT shaver system

Similar devices

Also classified as ENT shaver system.

Other devices from Karl Storz SE & CO. KG

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Properties

  • Prescription use
  • Serial number
Other properties (13, all answered No)