FDA UDI In Commercial Distribution 🇺🇸 United States

OneTouch Verio Flex

DI: 00353885012799 · Model: 024-336 · LifeScan Europe GmbH
Product Codes
2
GMDN Terms
1
Identifiers
3
Pkg Device Count
1

Basic Information

Brand Name
OneTouch Verio Flex
Primary DI
00353885012799
Version / Model
024-336
Catalog Number
024-336
Company Name
LifeScan Europe GmbH
Labeler DUNS
480240820
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2023-05-26
Public Version
1
Public Version Date
2023-06-05
Public Version Status
New
Public Device Record Key
9340d180-8935-4450-9741-a2090ee20738

Device Description

OneTouch Verio Flex Blood Glucose Monitoring System

Device Characteristics

Single Use
No
Prescription Use (Rx)
No
Over the Counter (OTC)
Yes
Kit
Yes
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
No
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
LFR Glucose Dehydrogenase, Glucose
NBW System, Test, Blood Glucose, Over The Counter

GMDN Terms

Code Name
62537 Glucose monitoring system IVD, home-use

Identifiers

Type ID
Package 20353885012793
Primary 00353885012799
Secondary 53885-336-01

Customer Contacts

Phone
8885673003

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
41 – 86 Degrees Fahrenheit
Type
Handling Environment Temperature
Temperature Range
50 – 104 Degrees Fahrenheit
Type
Handling Environment Humidity
Temperature Range
10 – 90 Percent (%) Relative Humidity