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27040GP40

by Karl Storz SE & CO. KG

27040GP40 is a Class II device made by Karl Storz SE & CO. KG, listed in FDA GUDID since 23 Sep 2016 (UDI-DI 04048551274156), 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 Number04048551274156 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  • Withdrawn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

Generic name
Endoscopic electrosurgical electrode, bipolar, reusable
Model / Ref / Catalog
27040GP40
Primary DI / UDI-DI
04048551274156
FDA product code
FAS
GMDN term
Endoscopic electrosurgical electrode, bipolar, reusable
Device class
Class II
Regulation number
876.4300
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

Related devices

Category: Endoscopic electrosurgical electrode, bipolar, reusable

Other devices from Karl Storz SE & CO. KG

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Properties

  • Sterilise before use
  • Prescription use
  • Lot / batch number
Other properties (12, all answered No)