SYSTEM 1E Liquid Chemical Sterilant Processing System - Placement Program 7500PLACE

GUDID 00724995152628

The SYSTEM 1E Liquid Chemical Sterilant Processing System is for safe and effective reprocessing of heat-sensitive critical and semi-critical medical devices. This unit is distributed through the STERIS Placement Program.

Corporation Steris Canada

Liquid sterilant sterilizer Liquid sterilant sterilizer Liquid sterilant sterilizer Liquid sterilant sterilizer Liquid sterilant sterilizer Liquid sterilant sterilizer Liquid sterilant sterilizer Liquid sterilant sterilizer Liquid sterilant sterilizer Liquid sterilant sterilizer Liquid sterilant sterilizer Liquid sterilant sterilizer Liquid sterilant sterilizer Liquid sterilant sterilizer Liquid sterilant sterilizer Liquid sterilant sterilizer Liquid sterilant sterilizer Liquid sterilant sterilizer Liquid sterilant sterilizer Liquid sterilant sterilizer Liquid sterilant sterilizer Liquid sterilant sterilizer Liquid sterilant sterilizer Liquid sterilant sterilizer Liquid sterilant sterilizer Liquid sterilant sterilizer Liquid sterilant sterilizer Liquid sterilant sterilizer Liquid sterilant sterilizer Liquid sterilant sterilizer Liquid sterilant sterilizer Liquid sterilant sterilizer Liquid sterilant sterilizer Liquid sterilant sterilizer Liquid sterilant sterilizer Liquid sterilant sterilizer Liquid sterilant sterilizer Liquid sterilant sterilizer Liquid sterilant sterilizer Liquid sterilant sterilizer Liquid sterilant sterilizer Liquid sterilant sterilizer Liquid sterilant sterilizer Liquid sterilant sterilizer Liquid sterilant sterilizer Liquid sterilant sterilizer Liquid sterilant sterilizer
Primary Device ID00724995152628
NIH Device Record Key20994f2f-2a02-4627-b2d5-9f51cd96d3e1
Commercial Distribution StatusIn Commercial Distribution
Brand NameSYSTEM 1E Liquid Chemical Sterilant Processing System - Placement Program
Version Model Number1E
Catalog Number7500PLACE
Company DUNS202659140
Company NameCorporation Steris Canada
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 Batchfalse
Serial Numbertrue
Manufacturing Datetrue
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
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
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
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
GS100724995152628 [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 Number6
Public Version Date2019-12-18
Device Publish Date2016-09-23

Devices Manufactured by Corporation Steris Canada

00724995217433 - enspire2024-04-25 The enspire 300 Series Automated Endoscope Reprocessor is designed to effectively test, clean, high level disinfect, rinse and a
00724995217440 - enspire2024-04-25 The enspire 300 Series Automated Endoscope Reprocessor is designed to effectively test, clean, high level disinfect, rinse and a
00724995217457 - enspire2024-04-25 The enspire 300 Series Automated Endoscope Reprocessor is designed to effectively test, clean, high level disinfect, rinse and a
00724995217464 - enspire2024-04-25 The enspire 300 Series Automated Endoscope Reprocessor is designed to effectively test, clean, high level disinfect, rinse and a
00724995217471 - enspire2024-04-25 The enspire 300 Series Automated Endoscope Reprocessor is designed to effectively test, clean, high level disinfect, rinse and a
00724995217488 - enspire2024-04-25 The enspire 300 Series Automated Endoscope Reprocessor is designed to effectively test, clean, high level disinfect, rinse and a
00724995217495 - enspire2024-04-25 The enspire 300 Series Automated Endoscope Reprocessor is designed to effectively test, clean, high level disinfect, rinse and a
00724995217501 - enspire2024-04-25 The enspire 3000 Series Automated Endoscope Reprocessor is designed to effectively test, clean, high level disinfect, rinse and

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.