OneTouch Ultrasoft 020-393

GUDID 20353885393106

OneTouch Ultrasoft Lancets

LifeScan Europe GmbH

Glucose monitoring system IVD, point-of-care

• Primary Device ID: 20353885393106
• NIH Device Record Key: 47e52ab8-a893-430b-8a9d-8f0bcd4c6b71
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: OneTouch Ultrasoft
• Version Model Number: 020-393
• Catalog Number: 020-393
• Company DUNS: 480240820
• Company Name: LifeScan Europe GmbH
• Device Count: 100
• 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: false
• 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: true

Customer Support Contacts

• Phone: +1 8002278862
• Email: XX@XX.XX

Device Dimensions

• Needle Gauge: 28 Gauge

Device Identifiers

Device Issuing Agency	Device ID
GS1	00353885393102 [Primary]
GS1	20353885393106 [Package]; Contains: 00353885393102; Package: Shipper case [24 Units]; In Commercial Distribution
NDC/NHRIC	53885-393-10 [Secondary]
GS1	80353885393108 [Unit of Use]

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: 2019-12-03
• Device Publish Date: 2019-11-25

On-Brand Devices [OneTouch Ultrasoft]

• 20353885393106: OneTouch Ultrasoft Lancets
• 20353885012441: OneTouch Ultrasoft Lancets