OneTouch Verio Flex 023-271

GUDID 20353885010980

OneTouch Verio Flex Blood Glucose Monitoring System. For in vitro diagnostic use. For self-testing

LifeScan Europe GmbH

Glucose monitoring system IVD, home-use

• Primary Device ID: 20353885010980
• NIH Device Record Key: 8e07100a-1d9b-4f02-9016-cbc850f66150
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: OneTouch Verio Flex
• Version Model Number: 023-271
• Catalog Number: 023-271
• Company DUNS: 480240820
• Company Name: LifeScan Europe GmbH
• 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: true
• Serial Number: true
• Manufacturing Date: true
• 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: true

Customer Support Contacts

• Phone: +1(888)567-3003
• Email: XX@XX.XX

Device Dimensions

• Device Size Text, specify: 0
• Device Size Text, specify: 0

Operating and Storage Conditions

• Special Storage Condition, Specify: Between 0 and 0 *Operating Altitude up to 10000 Feet
• Special Storage Condition, Specify: Between 0 and 0 *Operating Altitude up to 10000 Feet
• Special Storage Condition, Specify: Between 0 and 0 *Operating Altitude up to 10000 Feet
• Special Storage Condition, Specify: Between 0 and 0 *Operating Altitude up to 10000 Feet

Device Identifiers

Device Issuing Agency	Device ID
GS1	00353885010986 [Primary]
GS1	20353885010980 [Package]; Contains: 00353885010986; Package: Shipper case [32 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: 3
• Public Version Date: 2019-07-26
• Device Publish Date: 2017-09-13

On-Brand Devices [OneTouch Verio Flex]

• 20353885011765: OneTouch Verio Flex Blood Glucose Monitoring System. Uses the OneTouch Verio Test Strip. Not for
• 20353885010980: OneTouch Verio Flex Blood Glucose Monitoring System. For in vitro diagnostic use. For self-testi
• 20353885010973: OneTouch Verio Flex Blood Glucose Monitoring System. Uses the OneTouch Verio Test Strip. Not for
• 20353885010713: OneTouch Verio Flex Blood Glucose Monitoring System. Uses the OneTouch Verio Test Strip.
• 20353885011840: OneTouch Verio Flex Blood Glucose Monitoring System.
• 20353885011833: OneTouch Verio Flex Blood Glucose Monitoring System.
• 20353885012489: OneTouch Verio Flex Blood Glucose Monitoring System