Duns Number:141608724
Device Description: ACCU-CHEK AVIVA PLUS METER-ONLY
Catalog Number
06988601001
Brand Name
ACCU-CHEK AVIVA PLUS
Version/Model Number
06988601001
Device Commercial Distribution Status
Not in Commercial Distribution
Commercial Distribution End Date
August 29, 2018
Issuing Agency
In GS1
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
-
Product Code
NBW
Product Code Name
System, Test, Blood Glucose, Over The Counter
Public Device Record Key
efad36f1-438f-43b8-ad51-d4b7b7437843
Public Version Date
April 29, 2019
Public Version Number
3
DI Record Publish Date
August 26, 2016
Package DI Number
10365702102108
Quantity per Package
12
Contains DI Package
00365702102101
Package Discontinue Date
August 29, 2018
Package Status
Not in Commercial Distribution
Package Type
-
| 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 |