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Endomat UP210

by Karl Storz SE & CO. KG

Endomat UP210 is a Class II device made by Karl Storz SE & CO. KG, listed in FDA GUDID since 11 Jan 2020 (UDI-DI 04048551376041), 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 Number04048551376041 UDI-DI Date11 Jan 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  • Withdrawn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
Endomat
Generic name
Surgical irrigation/aspiration pump, reusable
Model / reference
UP210
Primary DI / UDI-DI
04048551376041
FDA product code
HIG
GMDN term
Surgical irrigation/aspiration pump, reusable
Device class
Class II
Regulation number
884.1700
GUDID distribution status
In Commercial Distribution

Related devices

Category: Surgical irrigation/aspiration pump, reusable

Similar devices in this category

Other devices filed under Surgical irrigation/aspiration pump, reusable.

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Properties

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