Accu-Chek Aviva - ACCU-CHEK AVIVA MG/DL 455 US NON-VA - Roche Diagnostics Operations, Inc.

Duns Number:141608724

Device Description: ACCU-CHEK AVIVA MG/DL 455 US NON-VA

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More Product Details

Catalog Number

-

Brand Name

Accu-Chek Aviva

Version/Model Number

08340331001

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

K133862

Product Code Details

Product Code

LFR

Product Code Name

Glucose Dehydrogenase, Glucose

Device Record Status

Public Device Record Key

c1e489fc-be96-41cb-9d97-2f815f1cdac1

Public Version Date

March 11, 2019

Public Version Number

1

DI Record Publish Date

February 28, 2019

Additional Identifiers

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-

"ROCHE DIAGNOSTICS OPERATIONS, INC." Characteristics
Device Class Device Class Description No of Devices
1 A medical device with low to moderate risk that requires general controls 4
2 A medical device with a moderate to high risk that requires special controls. 63
3 A medical device with high risk that requires premarket approval 3