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Coag Dissector 165 cm

by Ovesco Endoscopy AG

Coag Dissector 165 cm (200.50) is a Class II device made by Ovesco Endoscopy AG, cleared under FDA 510(k) K141794 on 19 Nov 2014 and listed in FDA GUDID since 5 Jul 2018 (UDI-DI 04260206311027), 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) K141794

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 Number04260206311027 UDI-DI Date5 Jul 2018ListedStatusListed GUDID: in commercial distribution
United StatesFDA 510(k)SESE from GUDID Substantially Equivalent · Traditional NumberK141794 Date19 Nov 2014DecidedStatusActive

Official records

Across registries

2 registries list this device

  • FDA 510(k) K141794 decided 19 Nov 2014 Active
  • FDA GUDID UDI-DI 04260206311027 listed 5 Jul 2018 Listed

Timeline

2 dated events

  1. Cleared FDA 510(k) K141794
  2. Listed FDA GUDID 04260206311027

Coverage

1 jurisdiction

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  • Withdrawn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

United States — FDA 510(k) Active

Specification

GUDID

Trade name
Coag Dissector
Generic name
Endoscopic electrosurgical handpiece/electrode, monopolar, single-use
Model / Ref / Catalog
165 cm, 200.50
Primary DI / UDI-DI
04260206311027
510(k) Number
FDA product code
KGE
GMDN term
Endoscopic electrosurgical handpiece/electrode, monopolar, single-use
Device class
Class II
Regulation number
876.4300
GUDID distribution status
In Commercial Distribution

Similar devices in this category

Other devices filed under Endoscopic electrosurgical handpiece/electrode, monopolar, single-use.

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Properties

  • Supplied sterile
  • Single use
  • Prescription use
  • Lot / batch number
  • Expiration date
  • Manufacturing date
Other properties (9, all answered No)