AccessGUDID - DEVICE: ACCU-CHEK AVIVA CONNECT (00365702593107)

GUDID

Device Identifier (DI) Information

Brand Name: ACCU-CHEK AVIVA CONNECT
Version or Model: 06979505001
Commercial Distribution Status: Not in Commercial Distribution
Catalog Number: 06979505001
Company Name: Roche Diagnostics Operations, Inc.

Primary DI Number: 00365702593107
Issuing Agency: GS1
Commercial Distribution End Date: April 29, 2020
Device Count: 1
Labeler D-U-N-S® Number*: 141608724 *Terms of Use

Device Description: ACCU-CHEK AVIVA CONNECT MG/DL (502)

Device Characteristics

What MRI safety information does the labeling contain?	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):	No
Device labeled as "Not made with natural rubber latex":	No
For Single-Use:	No
Prescription Use (Rx):	No
Over the Counter (OTC):	No
Kit:	No
Combination Product:	No
Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P):	No

GMDN

[?]

GMDN Term Code	GMDN Term Name	GMDN Term Definition	GMDN Term Status [?]	Implantable?
62645	Glucose analyser IVD, home-use	An electrically-powered instrument intended to be used for the quantitative in vitro measurement of glucose levels in whole blood; it is designed to be used for self-testing by a layperson in the home, and some types may in addition be used at the point-of-care. Measured glucose values are used to manage blood glucose levels, primarily by persons with diabetes mellitus. This analyser is typically included in a blood glucose monitoring system.	Active	false

FDA Product Code

[?]

Product Code	Product Code Name
NBW	System, Test, Blood Glucose, Over The Counter

FDA Premarket Submission

FDA Premarket Submission Number [?]	Supplement Number [?]
Premarket Submission Number Not Available/Not Released

Device Exempt from Premarket Submission: No CLOSE

Sterilization

Device Packaged as Sterile: No
Requires Sterilization Prior to Use: No

Sterilization Method [?]
No Sterilization Methods Found

Storage and Handling

[?]

Storage and Handling
No storage/handling found

Clinically Relevant Size

[?]

Size Type Text
No Device Sizes

Device Record Status

Public Device Record Key: 29cfbf6d-3327-4c4c-bf3e-470341835b16
Public Version Date: July 25, 2023
Public Version Number: 3
DI Record Publish Date: August 26, 2016