CONTOUR® NEXT 7312

GUDID 40301939737219

Blood Glucose Test Strips - 50 Test Strips (per bottle) - sold in a carton of 2 bottles (100 test strips total).

ASCENSIA DIABETES CARE US INC.

Glucose monitoring system IVD, home-use

• Primary Device ID: 40301939737219
• NIH Device Record Key: 44ed198d-216c-4ada-831a-b89354b8d201
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: CONTOUR® NEXT
• Version Model Number: 7312
• Catalog Number: 7312
• Company DUNS: 080028910
• Company Name: ASCENSIA DIABETES CARE US INC.
• Device Count: 50
• 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: true
• Lot Batch: true
• Serial Number: false
• Manufacturing Date: false
• Expiration Date: true
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: true
• OTC Over-The-Counter: true

Customer Support Contacts

• Phone: 18003488100
• Email: support@contournext.com

Operating and Storage Conditions

• Storage Environment Humidity: Between 10 Percent (%) Relative Humidity and 80 Percent (%) Relative Humidity

Device Identifiers

Device Issuing Agency	Device ID
GS1	00301937312014 [Unit of Use]
GS1	00301937312212 [Package]; Contains: 10301937312219; Package: carton [2 Units]; In Commercial Distribution
NDC/NHRIC	0193-7312-21 [Secondary]
GS1	10301937312219 [Primary]
GS1	40301935541049 [Package]; Contains: 00301937312212; Package: shipper / speed pack [4 Units]; In Commercial Distribution
GS1	40301937312210 [Package]; Contains: 00301937312212; Package: case [12 Units]; In Commercial Distribution
GS1	40301939737219 [Package]; Contains: 00301937312212; Package: case [12 Units]; In Commercial Distribution
GS1	40301939770513 [Package]; Contains: 00301937312212; Package: shipper/case [2 Units]; In Commercial Distribution

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K121190

FDA Product Code

• OZO: Artificial Pancreas Device System, Threshold Suspend

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 5
• Public Version Date: 2019-06-07
• Device Publish Date: 2016-08-25

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