FDA UDI In Commercial Distribution 🇺🇸 United States

One Touch SureSoft

DI: 00353885006835 · Model: 021-140 · LifeScan Europe GmbH
Product Codes
1
GMDN Terms
1
Identifiers
4
Pkg Device Count
200

Basic Information

Brand Name
One Touch SureSoft
Primary DI
00353885006835
Version / Model
021-140
Company Name
LifeScan Europe GmbH
Labeler DUNS
480240820
Distribution Status
In Commercial Distribution
Device Count in Pkg
200
Record Status
Published
Publish Date
2020-02-03
Public Version
1
Public Version Date
2020-02-11
Public Version Status
New
Public Device Record Key
9cef3b34-a2a6-465e-ad77-6c75454930b4

Device Description

One Touch SureSoft Single Use Disposable Lancing Device

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
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
Yes
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
Yes
Sterilization Methods
Radiation Sterilization

Product Codes

Code Name
FMK Lancet, Blood

GMDN Terms

Code Name
61578 Manual blood lancing device, single-use

Identifiers

Type ID
Package 20353885006839
Primary 00353885006835
Secondary 53885-140-20
Unit of Use 80353885006831

Device Sizes

Type Value Unit Text
Needle Gauge 28 Gauge