091271-06

GUDID 04048551428016

Video Uretero-Renoscope FLEX-XC1

Karl Storz GmbH & Co. KG

Flexible video ureterorenoscope, single-use
Primary Device ID04048551428016
NIH Device Record Keye35a47bc-58b2-496b-8c4d-777f176decc6
Commercial Distribution StatusIn Commercial Distribution
Version Model Number091271-06
Catalog Number091271-06
Company DUNS315731430
Company NameKarl Storz GmbH & Co. KG
Device Count6
DM Exemptfalse
Pre-market Exemptfalse
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usetrue
Lot Batchtrue
Serial Numberfalse
Manufacturing Datetrue
Expiration Datetrue
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Customer Support Contacts

Phone+14242188201
Emailregulatory@karlstorz.com
Phone+14242188201
Emailregulatory@karlstorz.com
Phone+14242188201
Emailregulatory@karlstorz.com
Phone+14242188201
Emailregulatory@karlstorz.com
Phone+14242188201
Emailregulatory@karlstorz.com
Phone+14242188201
Emailregulatory@karlstorz.com
Phone+14242188201
Emailregulatory@karlstorz.com
Phone+14242188201
Emailregulatory@karlstorz.com
Phone+14242188201
Emailregulatory@karlstorz.com
Phone+14242188201
Emailregulatory@karlstorz.com
Phone+14242188201
Emailregulatory@karlstorz.com
Phone+14242188201
Emailregulatory@karlstorz.com
Phone+14242188201
Emailregulatory@karlstorz.com

Device Identifiers

Device Issuing AgencyDevice ID
GS104048551428009 [Primary]
GS104048551428016 [Unit of Use]

FDA Product Code

FGBUreteroscope and accessories, flexible/rigid

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2025-04-04
Device Publish Date2025-03-27

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