QMC1800E

GUDID 00724995220266

The Quick Connect for SonoScape GI Endoscopes is used with with the Universal Flexible Processing Tray in the SYSTEM 1 E and SYSTEM 1 endo Liquid Chemical Sterilant Processing Systems.

STERIS CORPORATION

Luminal device flushing tubing set, reusable
Primary Device ID00724995220266
NIH Device Record Key882913f1-1c9f-4f91-9192-169e966c32a2
Commercial Distribution StatusIn Commercial Distribution
Version Model NumberQuick Connect
Catalog NumberQMC1800E
Company DUNS868205779
Company NameSTERIS CORPORATION
Device Count1
DM Exemptfalse
Pre-market Exemptfalse
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usefalse
Lot Batchtrue
Serial Numberfalse
Manufacturing Datefalse
Expiration Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptionfalse
OTC Over-The-Countertrue

Customer Support Contacts

Phone+1(800)548-4873
Emailxx@xx.xx
Phone+1(800)548-4873
Emailxx@xx.xx
Phone+1(800)548-4873
Emailxx@xx.xx
Phone+1(800)548-4873
Emailxx@xx.xx
Phone+1(800)548-4873
Emailxx@xx.xx
Phone+1(800)548-4873
Emailxx@xx.xx
Phone+1(800)548-4873
Emailxx@xx.xx
Phone+1(800)548-4873
Emailxx@xx.xx
Phone+1(800)548-4873
Emailxx@xx.xx
Phone+1(800)548-4873
Emailxx@xx.xx
Phone+1(800)548-4873
Emailxx@xx.xx
Phone+1(800)548-4873
Emailxx@xx.xx
Phone+1(800)548-4873
Emailxx@xx.xx
Phone+1(800)548-4873
Emailxx@xx.xx

Device Identifiers

Device Issuing AgencyDevice ID
GS100724995220266 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

MEDSterilant, medical devices

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number2
Public Version Date2023-10-31
Device Publish Date2023-01-09

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