FDA UDI In Commercial Distribution 🇺🇸 United States

Sterilance LDE3

DI: 06945630112898 · Model: 02-1903 · Sterilance Medical (Suzhou) Inc.
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
1

Basic Information

Brand Name
Sterilance LDE3
Primary DI
06945630112898
Version / Model
02-1903
Company Name
Sterilance Medical (Suzhou) Inc.
Labeler DUNS
554434897
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2022-07-13
Public Version
1
Public Version Date
2022-07-21
Public Version Status
New
Public Device Record Key
1c6b877b-d838-4fbd-93d1-6b37d475d8b0

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
No
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
No
Sterilization Prior Use
No

Product Codes

Code Name
FMK Single Use Only Blood Lancet With An Integral Sharps Injury Prevention Feature

GMDN Terms

Code Name
37243 Manual blood lancing device, reusable

Identifiers

Type ID
Package 16945630112895
Primary 06945630112898
Package 36945630112899