NA - The VERIFY General Purpose Steam Process - STERIS CORPORATION

Duns Number:961394798

Device Description: The VERIFY General Purpose Steam Process Indicator Tape adheres to both natural and synthe The VERIFY General Purpose Steam Process Indicator Tape adheres to both natural and synthetic materials commonly used in sterile processing. They are used to identify processed packs from unprocessed packs.

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More Product Details

Catalog Number

260010

Brand Name

NA

Version/Model Number

260010

Device Commercial Distribution Status

Not in Commercial Distribution

Commercial Distribution End Date

November 06, 2019

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)

Yes

Device labeled as "Not made with natural rubber latex"

-

For Single-Use

Yes

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

K003002,K003002

Product Code Details

Product Code

JOJ

Product Code Name

Indicator, physical/chemical sterilization process

Device Record Status

Public Device Record Key

0c118300-0b3a-493f-8bbd-47c5b2abd23a

Public Version Date

November 06, 2019

Public Version Number

6

DI Record Publish Date

September 09, 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