ACCU-CHEK AVIVA CONNECT 06979505001

GUDID 00365702593107

ACCU-CHEK AVIVA CONNECT MG/DL (502)

Roche Diagnostics Operations, Inc.

Home-use/point-of-care glucose analyser IVD, battery-powered

• Primary Device ID: 00365702593107
• NIH Device Record Key: 29cfbf6d-3327-4c4c-bf3e-470341835b16
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: ACCU-CHEK AVIVA CONNECT
• Version Model Number: 06979505001
• Catalog Number: 06979505001
• Company DUNS: 141608724
• Company Name: Roche Diagnostics Operations, Inc.
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: false
• MRI Safety Status: Labeling does not contain MRI Safety Information
• Human Cell/Tissue Product: false
• Device Kit: false
• Device Combination Product: false
• Single Use: false
• Lot Batch: false
• Serial Number: true
• Manufacturing Date: false
• Expiration Date: false
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: false
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	00365702593107 [Primary]

FDA Product Code

• NBW: System, Test, Blood Glucose, Over The Counter

Sterilization

• Steralize Prior To Use: false
• Device Is Sterile: false

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 2
• Public Version Date: 2018-03-29
• Device Publish Date: 2016-08-26

On-Brand Devices [ACCU-CHEK AVIVA CONNECT]

• 00365702593107: ACCU-CHEK AVIVA CONNECT MG/DL (502)
• 10365702578101: ACCU-CHEK AVIVA CONNECT MG/DL M-O
• 10365702577104: ACCU-CHEK AVIVA CONNECT RETAIL KIT 8/CASE
• 10365702576107: ACCU-CHEK AVIVA CONNECT SAMPLE KIT 16/CASE