SinuFIT 456122ZY

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	Number04048551003084 UDI-DI	Date4 Sep 2018Listed	StatusListed GUDID: in commercial distribution

Coverage

1 jurisdiction

Active
Expiring
Withdrawn
Listed
Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade Name: SinuFIT
Generic Name: Surgical soft-tissue manipulation forceps, scissors-like, reusable
Model / Reference: 456122ZY

Primary DI / UDI-DI: 04048551003084
FDA Product Code: LRC
GMDN Term: Surgical soft-tissue manipulation forceps, scissors-like, reusable

Device Class: Class I
Regulation Number: 874.4420
GUDID distribution status: In Commercial Distribution

Sterilization Method: Moist Heat or Steam Sterilization

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Properties

Prescription Use
Premarket Exempt
Serial Number

Other properties (11)

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