Easy Mini Eject Lancing Device 1171

GUDID 10891237001178

• Step-by-step instructions to acquire capillary blood sample. • Adjustable penetration depth • Maximum comfort • For use with most lancets

HOME AIDE DIAGNOSTICS, INC.

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Primary Device ID10891237001178
NIH Device Record Key0b0e28af-0a81-4be5-846b-1ea94835ab4d
Commercial Distribution StatusIn Commercial Distribution
Brand NameEasy Mini Eject Lancing Device
Version Model NumberLF-LDE
Catalog Number1171
Company DUNS783518983
Company NameHOME AIDE DIAGNOSTICS, 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 Usefalse
Lot Batchtrue
Serial Numberfalse
Manufacturing Datefalse
Expiration Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptionfalse
OTC Over-The-Countertrue

Customer Support Contacts

Phone18009150116
Emailinfo@homeaide.us
Phone18009150116
Emailinfo@homeaide.us
Phone18009150116
Emailinfo@homeaide.us
Phone18009150116
Emailinfo@homeaide.us
Phone18009150116
Emailinfo@homeaide.us
Phone18009150116
Emailinfo@homeaide.us
Phone18009150116
Emailinfo@homeaide.us
Phone18009150116
Emailinfo@homeaide.us
Phone18009150116
Emailinfo@homeaide.us
Phone18009150116
Emailinfo@homeaide.us
Phone18009150116
Emailinfo@homeaide.us
Phone18009150116
Emailinfo@homeaide.us
Phone18009150116
Emailinfo@homeaide.us

Device Identifiers

Device Issuing AgencyDevice ID
GS100891237001171 [Primary]
GS110891237001178 [Package]
Contains: 00891237001171
Package: Outer Case [100 Units]
In Commercial Distribution

FDA Product Code

FMKLancet, Blood

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number2
Public Version Date2022-11-29
Device Publish Date2018-08-03

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