FDA UDI In Commercial Distribution 🇺🇸 United States

OneTouch Verio

DI: 00353885007764 · Model: 022-273 · LifeScan Europe GmbH
Product Codes
2
GMDN Terms
1
Identifiers
3
Pkg Device Count
1

Basic Information

Brand Name
OneTouch Verio
Primary DI
00353885007764
Version / Model
022-273
Catalog Number
022-273
Company Name
LifeScan Europe GmbH
Labeler DUNS
480240820
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2019-11-25
Public Version
1
Public Version Date
2019-12-03
Public Version Status
New
Public Device Record Key
bb1a5a80-3bc6-449d-a25e-7ae9cf5570f5

Device Description

OneTouch Verio®Level 3 Control Solution

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
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
Yes
Has Expiration Date
Yes
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
62538 Glucose monitoring system IVD, point-of-care

Identifiers

Type ID
Secondary 53885-273-02
Primary 00353885007764
Package 20353885007768

Customer Contacts