FDA UDI In Commercial Distribution 🇺🇸 United States

OneTouch Verio

DI: 00353885009768 · Model: 022-899 · LifeScan Europe GmbH
Product Codes
2
GMDN Terms
1
Identifiers
4
Pkg Device Count
50

Basic Information

Brand Name
OneTouch Verio
Primary DI
00353885009768
Version / Model
022-899
Catalog Number
022-899
Company Name
LifeScan Europe GmbH
Labeler DUNS
480240820
Distribution Status
In Commercial Distribution
Device Count in Pkg
50
Record Status
Published
Publish Date
2017-09-13
Public Version
4
Public Version Date
2019-07-26
Public Version Status
Update
Public Device Record Key
0816ce16-f291-440b-97c2-eaf6358a0f64

Device Description

OneTouch Verio Blood Glucose Test Strips. In vitro Diagnostic. For Self-testing. Use with OneTouch Verio Family of Meters

Device Characteristics

Single Use
Yes
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
No
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
53303 Glucose IVD, kit, electrometry

Identifiers

Type ID
Package 20353885009762
Primary 00353885009768
Unit of Use 80353885009764
Secondary 53885-271-50

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K110637 000
K120708 000
K131363 000

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
41 – 86 Degrees Fahrenheit
Type
Special Storage Condition, Specify
Special Conditions
Discard 6 months after opening
Type
Special Storage Condition, Specify
Special Conditions
Store your test strips in the vial only