ACCU-CHEK CONNECT

GUDID 00365702700017

ACCU-CHEK CONNECT DIABETES MANAGEMENT AP

Roche Diagnostics Operations, Inc.

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• Primary Device ID: 00365702700017
• NIH Device Record Key: 1ac106ee-9805-471a-8420-65eba124c1a9
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: ACCU-CHEK CONNECT
• Version Model Number: 07250452001
• 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: false
• 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	00365702700017 [Primary]

FDA Product Code

• NDC: Calculator, Drug Dose

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: 2016-09-13

On-Brand Devices [ACCU-CHEK CONNECT]

• 00365702700017: ACCU-CHEK CONNECT DIABETES MANAGEMENT AP
• 00365702700000: ACCU-CHEK CONNECT DIABETES MGMT iAP