n.a. 26183MR

by Karl Storz SE & CO. KG

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

Registry data, not yet checked by deviCERTS. Source GUDID, synced 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

Region	Authorization	Number	Date	Status
United States	GUDID listing	Number04048551347645 UDI-DI	Date22 Dec 2016Listed	StatusListed GUDID: in commercial distribution

Coverage

1 jurisdiction

Active
Expiring
Withdrawn
Listed
Not covered

United States — GUDID listing Listed

Specification

GUDID

Generic Name: Endoscopic electrosurgical electrode, monopolar, single-use
Model / Ref / Catalog: 26183MR

Primary DI / UDI-DI: 04048551347645
FDA Product Code: KNF
GMDN Term: Endoscopic electrosurgical electrode, monopolar, single-use

Device Class: Class II
Regulation Number: 884.4160
GUDID distribution status: In Commercial Distribution

Sterilization Method: Moist Heat or Steam Sterilization

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Properties

Single Use
Prescription Use

Other properties (12)

Sterile: No
Implantable: No
Contains Latex: No
Over-the-Counter: No
Convenience Kit: No
Combination Product: No
HCT/P: No
Premarket Exempt: No
Lot / Batch Number: No
Serial Number: No
Expiration Date: No
Manufacturing Date: No