FDA UDI In Commercial Distribution 🇺🇸 United States

Sterilance Press Plus Safety Lancet 26G 1.8mm

DI: 16945630123150 · Model: 05-232618 · Sterilance Medical (Suzhou) Inc.
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
100

Basic Information

Brand Name
Sterilance Press Plus Safety Lancet 26G 1.8mm
Primary DI
16945630123150
Version / Model
05-232618
Company Name
Sterilance Medical (Suzhou) Inc.
Labeler DUNS
554434897
Distribution Status
In Commercial Distribution
Device Count in Pkg
100
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
b8a9ee02-6ead-4e98-976e-dd206a8c9cc1

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

GMDN Terms

Code Name
61578 Manual blood lancing device, single-use

Identifiers

Type ID
Package 36945630123154
Primary 16945630123150
Unit of Use 06945630123153