844321

by Karl Storz SE & CO. KG

844321 is a Class II device made by Karl Storz SE & CO. KG, listed in FDA GUDID since 17 Aug 2018 (UDI-DI 04048551208472), 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

Source GUDID, synced 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

Region	Authorization	Number	Date	Status
United States	GUDID listing	Number04048551208472 UDI-DI	Date17 Aug 2018Listed	StatusListed GUDID: in commercial distribution

Official records

AccessGUDID record UDI-DI 04048551208472

Coverage

1 jurisdiction

Active
Expiring
Withdrawn
Listed
Not covered

United States — GUDID listing Listed

Specification

GUDID

Generic name: Endoscopic electrosurgical electrode, bipolar, reusable
Model / reference: 844321

Primary DI / UDI-DI: 04048551208472
FDA product code: EOB
GMDN term: Endoscopic electrosurgical electrode, bipolar, reusable

Device class: Class II
Regulation number: 874.4760
GUDID distribution status: In Commercial Distribution

Sterilisation method: Moist Heat or Steam Sterilization

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Properties

Sterilise before use
Prescription use
Lot / batch number

Other properties (12, all answered No)