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142700

by Karl Storz SE & CO. KG

Ref 142700

142700 is a Class I device made by Karl Storz SE & CO. KG, registered in EUDAMED on 19 May 2026 (Basic UDI-DI 4048551002021T2) and listed in FDA GUDID since 23 Feb 2019 (UDI-DI 04048551057315), withdrawn as of 22 Oct 2026.

Withdrawn Withdrawn in European Union.

Was authorized under CE MDR, withdrawn

Ended

Withdrawn

Date not published (CE MDR)

FDA recalls

Not checked

No FDA submission to match recalls against

Documents

None linked in EUDAMED

A group certificate may exist

Trust

Unverified

Source EUDAMED, GUDID, synced 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR EUDAMED Number4048551002021T2 Basic UDI-DI 04048551057315UDI-DIDate19 May 2026RegisteredStatusWithdrawn
United StatesGUDID listing GUDID Number04048551057315 UDI-DI Date23 Feb 2019ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI 4048551002021T2 registered 19 May 2026 Withdrawn
  • FDA GUDID UDI-DI 04048551057315 listed 23 Feb 2019 Listed

Timeline

2 dated events

  1. Listed FDA GUDID 04048551057315
  2. Registered EUDAMED 4048551002021T2

Coverage

2 jurisdictions

United States of AmericaSwedenFinlandLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaAustriaHungaryRomaniaSloveniaBulgariaPortugalSpainItalyCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered
  • European Union CE/MDR Withdrawn
  • United States GUDID listing Listed

Specification

EUDAMED · GUDID

Generic name
Eustachian catheter, reusable
Device name
Connectors
Model / Ref / Catalog
142700
Primary DI / UDI-DI
04048551057315
Basic UDI-DI
4048551002021T2
FDA product code
KCL
EMDN code
L140599 Ear surgery instruments, reusable - other
GMDN term
Eustachian catheter, reusable
Device class
Class I
Regulation number
874.5220
EU registration type
Standard device
EU market of registration
Germany
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

Related devices

Category: Eustachian catheter, reusable

Similar devices in this category

Other devices filed under EAR SURGERY INSTRUMENTS, REUSABLE - OTHER.

Other devices from Karl Storz SE & CO. KG

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Properties

  • Sterilise before use
  • Prescription use
  • Premarket exempt
  • Lot / batch number
Other properties (21, all answered No)