FDA UDI In Commercial Distribution 🇺🇸 United States

STERiLANCE

DI: 16945630141994 · Model: Press2 26G 1.8mm · Sterilance Medical (Suzhou) Inc.
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
100

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Basic Information

Brand Name
STERiLANCE
Primary DI
16945630141994
Version / Model
Press2 26G 1.8mm
Company Name
Sterilance Medical (Suzhou) Inc.
Labeler DUNS
554434897
Distribution Status
In Commercial Distribution
Device Count in Pkg
100
Record Status
Published
Publish Date
2026-03-09
Public Version
1
Public Version Date
2026-03-17
Public Version Status
New
Public Device Record Key
9d7188d4-b205-475e-a28c-e7d8b4566425

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
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
Unit of Use 06945630141997
Primary 16945630141994
Package 36945630141998