FDA UDI In Commercial Distribution 🇺🇸 United States

OneTouch Verio Flex

DI: 00353885010986 · Model: 023-271 · LifeScan Europe GmbH
Product Codes
2
GMDN Terms
2
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
OneTouch Verio Flex
Primary DI
00353885010986
Version / Model
023-271
Catalog Number
023-271
Company Name
LifeScan Europe GmbH
Labeler DUNS
480240820
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2017-09-13
Public Version
3
Public Version Date
2019-07-26
Public Version Status
Update
Public Device Record Key
8e07100a-1d9b-4f02-9016-cbc850f66150

Device Description

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

Device Characteristics

Single Use
No
Prescription Use (Rx)
No
Over the Counter (OTC)
Yes
Kit
No
Combination Product
No
HCT/P
No
Contains NRL
No
Not Made with NRL
No
MRI Safety
Labeling does not contain MRI Safety Information
Direct Marking Exempt
No
PM Exempt
No
Has Serial Number
Yes
Has Lot/Batch Number
Yes
Has Manufacturing Date
Yes
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
NBW SYSTEM, TEST, BLOOD GLUCOSE, OVER THE COUNTER
LFR Glucose dehydrogenase, glucose

GMDN Terms

Code Name
62537 Glucose monitoring system IVD, home-use
62645 Glucose analyser IVD, home-use

Identifiers

Type ID
Package 20353885010980
Primary 00353885010986

Customer Contacts

Device Sizes

Type Value Unit Text
Device Size Text, specify Hematocrit 20 - 60%
Device Size Text, specify Blood Glucose measurement Level mg/dL

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
High: 86 Degrees Fahrenheit
Type
Handling Environment Temperature
Temperature Range
50 – 104 Degrees Fahrenheit
Type
Handling Environment Humidity
Temperature Range
10 – 90 Percent (%) Relative Humidity
Type
Special Storage Condition, Specify
Special Conditions
Operating Altitude up to 10000 Feet