Reliance - The Reliance EPS Processor is intended for - Corporation Steris Canada

Duns Number:202659140

Device Description: The Reliance EPS Processor is intended for washing and high Level disinfection of up to tw The Reliance EPS Processor is intended for washing and high Level disinfection of up to two manually pre-cleaned, immersible, reusable, heat-sensitive, semi-critical devices such as GI flexible endoscopes, bronchoscopes and their accessories.

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More Product Details

Catalog Number

MB3

Brand Name

Reliance

Version/Model Number

EPS

Device Commercial Distribution Status

Not in Commercial Distribution

Commercial Distribution End Date

October 28, 2022

Issuing Agency

In GS1

Product Characteristics

MRI safety Status

Labeling does not contain MRI Safety Information

Device required to be labeled as containing natural rubber latex or dry natural rubber (21 CFR 801.437)

-

Device labeled as "Not made with natural rubber latex"

-

For Single-Use

-

Prescription Use (Rx)

-

Over the Counter (OTC)

-

Kit

-

Combination Product

-

Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P)

-

FDA Premarket Submission

K040049,K102244,K200989,K203223,K220361

Product Code Details

Product Code

NZA

Product Code Name

Accessories, germicide, cleaning, for endoscopes

Device Record Status

Public Device Record Key

5944befc-03aa-47ed-a957-cfe10c5fe120

Public Version Date

October 31, 2022

Public Version Number

9

DI Record Publish Date

September 13, 2016

Additional Identifiers

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-

"CORPORATION STERIS CANADA" Characteristics
Device Class Device Class Description No of Devices
1 A medical device with low to moderate risk that requires general controls 58
2 A medical device with a moderate to high risk that requires special controls. 262