Abbott 70901

GUDID 30357599000692

Abbott SF Single Use Lancing Device

ABBOTT DIABETES CARE INC

Glucose monitoring system IVD, home-use

• Primary Device ID: 30357599000692
• NIH Device Record Key: 243021ce-0f42-407f-a2d3-958523fa47b6
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Abbott
• Version Model Number: 70901
• Catalog Number: 70901
• Company DUNS: 966390890
• Company Name: ABBOTT DIABETES CARE INC
• Device Count: 200
• DM Exempt: false
• Pre-market Exempt: true
• 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: true
• Manufacturing Date: true
• 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

Customer Support Contacts

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Device Identifiers

Device Issuing Agency	Device ID
GS1	00357599000691 [Primary]
GS1	10357599000698 [Unit of Use]
GS1	30357599000692 [Package]; Contains: 00357599000691; Package: Case [20 Units]; In Commercial Distribution
NDC/NHRIC	99073-0709-01 [Secondary]

FDA Product Code

• FMK: Lancet, blood

Sterilization

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

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2018-07-16
• Device Publish Date: 2018-06-15

On-Brand Devices [Abbott]

• 30357599000692: Abbott SF Single Use Lancing Device
• 30699073000843: Abbott Diabetes Care USB Data Cable Software
• 30093815000830: Abbott Diabetes Care USB Data Cable Software
• 30699073709012: Abbott SF Single Use Lancing Device
• 30699073708510: Abbott Diabetes Care USB Data Cable Software
• 30093815708453: Abbott Diabetes Care USB Data Cable Software