Libre App 78745-01

GUDID 00357599840006

Libre Android App US

ABBOTT DIABETES CARE INC

Percutaneous interstitial-fluid glucose monitoring system, electrochemical
Primary Device ID00357599840006
NIH Device Record Key5e485d6b-99bb-4dbc-92a7-0d2236c36d7d
Commercial Distribution StatusIn Commercial Distribution
Brand NameLibre App
Version Model Number78745-01
Catalog Number78745-01
Company DUNS966390890
Company NameABBOTT DIABETES CARE INC
Device Count1
DM Exemptfalse
Pre-market Exemptfalse
MRI Safety StatusMR Conditional
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usetrue
Lot Batchfalse
Serial Numberfalse
Manufacturing Datefalse
Expiration Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptionfalse
OTC Over-The-Counterfalse

Customer Support Contacts

Phone+1(855)632-8658
Emailxx@xx.xx
Phone+1(855)632-8658
Emailxx@xx.xx
Phone+1(855)632-8658
Emailxx@xx.xx
Phone+1(855)632-8658
Emailxx@xx.xx
Phone+1(855)632-8658
Emailxx@xx.xx
Phone+1(855)632-8658
Emailxx@xx.xx
Phone+1(855)632-8658
Emailxx@xx.xx
Phone+1(855)632-8658
Emailxx@xx.xx
Phone+1(855)632-8658
Emailxx@xx.xx
Phone+1(855)632-8658
Emailxx@xx.xx
Phone+1(855)632-8658
Emailxx@xx.xx
Phone+1(855)632-8658
Emailxx@xx.xx
Phone+1(855)632-8658
Emailxx@xx.xx
Phone+1(855)632-8658
Emailxx@xx.xx
Phone+1(855)632-8658
Emailxx@xx.xx
Phone+1(855)632-8658
Emailxx@xx.xx
Phone+1(855)632-8658
Emailxx@xx.xx
Phone+1(855)632-8658
Emailxx@xx.xx

Device Identifiers

Device Issuing AgencyDevice ID
GS100357599840006 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

QBJIntegrated Continuous Glucose Monitoring system, factory calibrated

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2024-12-25
Device Publish Date2024-12-17

On-Brand Devices [Libre App]

00357599841003Libre IOS App US
00357599840006Libre Android App US

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