ACCU-CHEK AVIVA CONNECT 07049811001

GUDID 10365702578101

ACCU-CHEK AVIVA CONNECT MG/DL M-O

Roche Diagnostics Operations, Inc.

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• Primary Device ID: 10365702578101
• NIH Device Record Key: ee703dd2-c2af-46c8-90d6-e7433274cf6d
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: ACCU-CHEK AVIVA CONNECT
• Version Model Number: 07049811001
• Catalog Number: 07049811001
• 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: true
• Device Combination Product: false
• Single Use: false
• Lot Batch: true
• Serial Number: true
• Manufacturing Date: false
• Expiration Date: true
• 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	00365702578104 [Primary]
GS1	10365702578101 [Package]; Contains: 00365702578104; Package: [8 Units]; In Commercial Distribution

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