FDA UDI In Commercial Distribution 🇺🇸 United States

SteriLance OneStep

DI: 16945630123488 · Model: 02-2401 · Sterilance Medical (Suzhou) Inc.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
SteriLance OneStep
Primary DI
16945630123488
Version / Model
02-2401
Company Name
Sterilance Medical (Suzhou) Inc.
Labeler DUNS
554434897
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2024-01-15
Public Version
1
Public Version Date
2024-01-23
Public Version Status
New
Public Device Record Key
d4055af5-8bb9-4ad7-a78f-6a623b566318

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
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
Yes
Sterilization Prior Use
No

Product Codes

Code Name
QRL Multiple Use Blood Lancet For Single Patient Use Only

GMDN Terms

Code Name
37243 Manual blood lancing device, reusable

Identifiers

Type ID
Package 36945630123482
Primary 16945630123488