STERiLANCE Press2 Disposable Safety Lancet

GUDID 36945630132491

Sterilance Medical (Suzhou) Inc.

Manual blood lancing device, single-use
Primary Device ID36945630132491
NIH Device Record Keyffc72b7a-1d32-491a-8b4c-d81a2c81129b
Commercial Distribution StatusIn Commercial Distribution
Brand NameSTERiLANCE Press2 Disposable Safety Lancet
Version Model Number05-062812
Company DUNS554434897
Company NameSterilance Medical (Suzhou) Inc.
Device Count100
DM Exemptfalse
Pre-market Exemptfalse
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usetrue
Lot Batchtrue
Serial Numberfalse
Manufacturing Datetrue
Expiration Datetrue
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latextrue
RX Perscriptionfalse
OTC Over-The-Countertrue

Device Identifiers

Device Issuing AgencyDevice ID
GS106945630132490 [Unit of Use]
GS116945630132497 [Primary]
GS136945630132491 [Package]
Contains: 16945630132497
Package: [10 Units]
In Commercial Distribution

FDA Product Code

FMKSingle Use Only Blood Lancet With An Integral Sharps Injury Prevention Feature

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2024-10-31
Device Publish Date2024-10-23

On-Brand Devices [STERiLANCE Press2 Disposable Safety Lancet]

3694563011508105-063018
3694563011507405-062818
3694563013108105-063018
3694563013240805-062122
3694563013239205-062122
3694563013250705-063012
3694563013249105-062812
3694563013248405-062620
3694563013247705-062118

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