SteriScan - The SteriScan Reusable Test Pack includes 2 test - STERIS CORPORATION

Duns Number:040469731

Device Description: The SteriScan Reusable Test Pack includes 2 test packs, 200 VERIFY STEAM Integrating Indic The SteriScan Reusable Test Pack includes 2 test packs, 200 VERIFY STEAM Integrating Indicators and 200 VERIFY All-In-One Bowie Dick Indicator Strips.

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More Product Details

Catalog Number

3300NC

Brand Name

SteriScan

Version/Model Number

3300NC

Device Commercial Distribution Status

In Commercial Distribution

Commercial Distribution End Date

-

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)

Yes

Kit

-

Combination Product

-

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

-

FDA Premarket Submission

-

Product Code Details

Product Code

FRC

Product Code Name

Indicator, biological sterilization process

Device Record Status

Public Device Record Key

8333f1bd-1751-41dd-b90e-61749d9e4552

Public Version Date

February 19, 2021

Public Version Number

4

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

-

"STERIS CORPORATION" Characteristics
Device Class Device Class Description No of Devices
1 A medical device with low to moderate risk that requires general controls 1528
2 A medical device with a moderate to high risk that requires special controls. 1557