Streptex Extraction Enzyme - REMEL EUROPE LIMITED

Duns Number:232600853

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More Product Details

Catalog Number

-

Brand Name

Streptex Extraction Enzyme

Version/Model Number

R30951001

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)

-

Kit

-

Combination Product

-

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

-

FDA Premarket Submission

K842828

Product Code Details

Product Code

JTO

Product Code Name

Discs, Strips And Reagents, Microorganism Differentiation

Device Record Status

Public Device Record Key

a4841687-b325-4f5e-b53d-7330e69360f0

Public Version Date

July 29, 2021

Public Version Number

1

DI Record Publish Date

July 21, 2021

Additional Identifiers

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-

"REMEL EUROPE LIMITED" Characteristics
Device Class Device Class Description No of Devices
1 A medical device with low to moderate risk that requires general controls 67
2 A medical device with a moderate to high risk that requires special controls. 124