Accu-Chek Compact Plus 05599423160

GUDID 00075537546611

Accu-Chek Compact Plus MIC 1x17 Str

Roche Diabetes Care GmbH

Home-use/point-of-care glucose analyser IVD, battery-powered Glucose IVD, reagent Glucose IVD, reagent Glucose IVD, reagent Glucose IVD, reagent Glucose IVD, reagent Glucose IVD, reagent Glucose IVD, reagent Glucose IVD, reagent Glucose IVD, reagent Glucose IVD, reagent Glucose IVD, reagent Glucose IVD, reagent Glucose IVD, reagent Glucose IVD, reagent Glucose IVD, reagent
Primary Device ID00075537546611
NIH Device Record Key87be1352-397e-41e8-9aef-93171b69928c
Commercial Distribution StatusIn Commercial Distribution
Brand NameAccu-Chek Compact Plus
Version Model Number05599423160
Catalog Number05599423160
Company DUNS313212471
Company NameRoche Diabetes Care GmbH
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 Datetrue
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptionfalse
OTC Over-The-Counterfalse

Device Identifiers

Device Issuing AgencyDevice ID
GS100075537546611 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

LFRGlucose Dehydrogenase, Glucose

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number3
Public Version Date2018-07-06
Device Publish Date2016-08-25

On-Brand Devices [Accu-Chek Compact Plus]

00365702468108Accu-Chek Compact Plus Clear Control USA
00075537927144ACCU-CHEK COMPACT PLUS 51 CT MO STRP 48
00075537598849ACCU-CHEK COMPACT PLUS 102CT RTL STR 24
00075537546611Accu-Chek Compact Plus MIC 1x17 Str
00075537474198ACCU-CHEK COMPACT PLUS 51 CT RTL STR 48

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.