FDA UDI In Commercial Distribution 🇺🇸 United States

OneTouch Ultra Plus Flex

DI: 00353885012836 · Model: 024-366 · LifeScan Europe GmbH
Product Codes
2
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
OneTouch Ultra Plus Flex
Primary DI
00353885012836
Version / Model
024-366
Catalog Number
024-366
Company Name
LifeScan Europe GmbH
Labeler DUNS
480240820
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2024-01-31
Public Version
1
Public Version Date
2024-02-08
Public Version Status
New
Public Device Record Key
b1d95dfc-1d38-405a-8899-da7a98d7ad55

Device Description

OneTouch Ultra Plus Flex™ Blood Glucose Monitoring System

Device Characteristics

Single Use
Yes
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
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 20353885012830
Primary 00353885012836