Accu-Chek Compact Plus - Accu-Chek Compact Plus Clear Control USA - Roche Diabetes Care GmbH

Duns Number:313212471

Device Description: Accu-Chek Compact Plus Clear Control USA

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More Product Details

Catalog Number

05888948160

Brand Name

Accu-Chek Compact Plus

Version/Model Number

05888948160

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

K113614,K113614

Product Code Details

Product Code

LFR

Product Code Name

Glucose Dehydrogenase, Glucose

Device Record Status

Public Device Record Key

5c179bea-e619-45cf-9f7f-9342fd3c0af9

Public Version Date

July 06, 2018

Public Version Number

3

DI Record Publish Date

August 26, 2016

Additional Identifiers

Package DI Number

10365702468105

Quantity per Package

6

Contains DI Package

00365702468108

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

-

"ROCHE DIABETES CARE GMBH" Characteristics
Device Class Device Class Description No of Devices
2 A medical device with a moderate to high risk that requires special controls. 16