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 ID20353885010980
NIH Device Record Key8e07100a-1d9b-4f02-9016-cbc850f66150
Commercial Distribution StatusIn Commercial Distribution
Brand NameOneTouch Verio Flex
Version Model Number023-271
Catalog Number023-271
Company DUNS480240820
Company NameLifeScan Europe GmbH
Device Count1
DM Exemptfalse
Pre-market Exemptfalse
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usefalse
Lot Batchtrue
Serial Numbertrue
Manufacturing Datetrue
Expiration Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptionfalse
OTC Over-The-Countertrue

Customer Support Contacts

Phone+1(888)567-3003
EmailXX@XX.XX

Device Dimensions

Device Size Text, specify0
Device Size Text, specify0

Operating and Storage Conditions

Special Storage Condition, SpecifyBetween 0 and 0 *Operating Altitude up to 10000 Feet
Special Storage Condition, SpecifyBetween 0 and 0 *Operating Altitude up to 10000 Feet
Special Storage Condition, SpecifyBetween 0 and 0 *Operating Altitude up to 10000 Feet
Special Storage Condition, SpecifyBetween 0 and 0 *Operating Altitude up to 10000 Feet

Device Identifiers

Device Issuing AgencyDevice ID
GS100353885010986 [Primary]
GS120353885010980 [Package]
Contains: 00353885010986
Package: Shipper case [32 Units]
In Commercial Distribution

FDA Product Code

NBWSYSTEM, TEST, BLOOD GLUCOSE, OVER THE COUNTER

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number3
Public Version Date2019-07-26
Device Publish Date2017-09-13

On-Brand Devices [OneTouch Verio Flex]

20353885011765OneTouch Verio Flex Blood Glucose Monitoring System. Uses the OneTouch Verio Test Strip. Not for
20353885010980OneTouch Verio Flex Blood Glucose Monitoring System. For in vitro diagnostic use. For self-testi
20353885010973OneTouch Verio Flex Blood Glucose Monitoring System. Uses the OneTouch Verio Test Strip. Not for
20353885010713OneTouch Verio Flex Blood Glucose Monitoring System. Uses the OneTouch Verio Test Strip.
20353885011840OneTouch Verio Flex Blood Glucose Monitoring System.
20353885011833OneTouch Verio Flex Blood Glucose Monitoring System.
20353885012489OneTouch Verio Flex Blood Glucose Monitoring System
20353885012793OneTouch Verio Flex Blood Glucose Monitoring System

Trademark Results [OneTouch Verio Flex]

Mark Image

Registration | Serial
Company
Trademark
Application Date
ONETOUCH VERIO FLEX
ONETOUCH VERIO FLEX
86468482 4999116 Live/Registered
Johnson & Johnson
2014-12-02

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