Disposable Safety Lancet Press2

GUDID 26945630125120

Sterilance Medical (Suzhou) Inc.

Manual blood lancing device, single-use
Primary Device ID26945630125120
NIH Device Record Key440fae1b-bb98-457e-9115-764dc4431393
Commercial Distribution StatusIn Commercial Distribution
Brand NameDisposable Safety Lancet Press2
Version Model Number05-062618
Company DUNS554434897
Company NameSterilance Medical (Suzhou) Inc.
Device Count1
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
GS106945630125126 [Primary]
GS126945630125120 [Package]
Contains: 06945630125126
Package: [100 Units]
In Commercial Distribution
GS136945630125127 [Package]
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 Date2024-04-08
Device Publish Date2024-03-31

Devices Manufactured by Sterilance Medical (Suzhou) Inc.

36945630132439 - STERiLANCE Elite Disposable Safety Lancet2024-10-31
36945630132446 - STERiLANCE Elite Disposable Safety Lancet2024-10-31
36945630132460 - STERiLANCE Elite Disposable Safety Lancet2024-10-31
36945630132477 - STERiLANCE Press2 Disposable Safety Lancet2024-10-31
36945630132484 - STERiLANCE Press2 Disposable Safety Lancet2024-10-31
36945630132491 - STERiLANCE Press2 Disposable Safety Lancet2024-10-31
36945630132507 - STERiLANCE Press2 Disposable Safety Lancet2024-10-31
36945630132514 - STERiLANCE Flex3 Disposable Safety Lancet2024-10-31

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