FDA UDI In Commercial Distribution 🇺🇸 United States

OneTouch Ultrasoft

DI: 00353885393102 · Model: 020-393 · LifeScan Europe GmbH
Product Codes
1
GMDN Terms
1
Identifiers
4
Pkg Device Count
100

Basic Information

Brand Name
OneTouch Ultrasoft
Primary DI
00353885393102
Version / Model
020-393
Catalog Number
020-393
Company Name
LifeScan Europe GmbH
Labeler DUNS
480240820
Distribution Status
In Commercial Distribution
Device Count in Pkg
100
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
47e52ab8-a893-430b-8a9d-8f0bcd4c6b71

Device Description

OneTouch Ultrasoft Lancets

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
Yes
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
No
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
FMK Lancet, Blood

GMDN Terms

Code Name
62538 Glucose monitoring system IVD, point-of-care

Identifiers

Type ID
Package 20353885393106
Primary 00353885393102
Secondary 53885-393-10
Unit of Use 80353885393108

Customer Contacts

Device Sizes

Type Value Unit Text
Needle Gauge 28 Gauge