n.a. 28162Z

by Karl Storz SE & CO. KG GUDID

Listed FDA GUDID listing, no authorization on record

Regulatory status

as of 29 Oct 2026

Region	Authorization	Number	Date	Status
United States	GUDID listing	Number04048551098561 UDI-DI	Date23 Sep 2016Listed	StatusListed GUDID: in commercial distribution

Coverage

1 jurisdiction

Active
Expiring
Withdrawn
Listed
Not covered

United States — GUDID listing Listed

Recalls

0 recalls · FDA

No FDA recalls on record, checked 22 Oct 2026.

Specification

GUDID

Generic Name: Rigid endoscopic biopsy forceps, reusable
Model / Ref / Catalog: 28162Z

Primary DI / UDI-DI: 04048551098561
FDA Product Code: GWG
GMDN Term: Rigid endoscopic biopsy forceps, reusable

Device Class: Class II
Regulation Number: 882.1480
GUDID distribution status: In Commercial Distribution

Sterilization Method: Moist Heat or Steam Sterilization

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Properties

Prescription Use
Lot / Batch Number

Other properties (12)

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