FDA UDI In Commercial Distribution 🇺🇸 United States

OneTouch Verio Reflect

DI: 00353885011723 · Model: 023-900 · LifeScan Europe GmbH
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
OneTouch Verio Reflect
Primary DI
00353885011723
Version / Model
023-900
Company Name
LifeScan Europe GmbH
Labeler DUNS
480240820
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2020-02-28
Public Version
1
Public Version Date
2020-03-09
Public Version Status
New
Public Device Record Key
aa6da7ce-dfe6-4911-ba72-e098fb67648c

Device Description

OneTouch Verio Reflect Blood Glucose Monitoring System. Warranty Kit

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
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

GMDN Terms

Code Name
62537 Glucose monitoring system IVD, home-use

Identifiers

Type ID
Package 20353885011727
Primary 00353885011723

Premarket Submissions

Submission Number Supplement Number
K193475 000

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
41 – 86 Degrees Fahrenheit
Type
Handling Environment Temperature
Temperature Range
43 – 111 Degrees Fahrenheit
Type
Handling Environment Humidity
Temperature Range
10 – 90 Degrees Fahrenheit
Type
Special Storage Condition, Specify
Special Conditions
keep away from direct sunlight and heat