38 results · 35ms · Sources: EU EUDAMED, US FDA

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CoaguSense Inc.

Manufacturer
🇺🇸 United States·4 Basic UDI-DIs·4 Devices·BSI Assurance UK Ltd, BSI Assurance UK Ltd, and BSI Assurance UK Ltd

COAGUSENSE INC

FDA registration
COAGUSENSE INC·3 products·🇺🇸 United States

Coag-Sense Prothrombin Time (PT) /INR Monitoring System

Device
EU IVDD · Eu Ivd General ·CoaguSense Inc.·On the market

Coag-Sense Prothrombin Time (PT)/INR Test Strip Kit

Device
EU IVDD · Eu Ivd General ·CoaguSense Inc.·On the market

Coag-Sense Prothrombin Time (PT)/INR Test Strip Kit

Device
EU IVDD · Eu Ivd General ·CoaguSense Inc.·On the market

Coag-Sense Control Test Strip Kit - 10 Count

Device
EU IVDD · Eu Ivd General ·CoaguSense Inc.·On the market

Coag-Sense PT/INR Patient Self-Test System

FDA UDI
COAGUSENSE INC.·00861900000381·Coag-Sense PT/INR Patient Self-Test System

Coag-Sense PT/INR Meter

FDA UDI
COAGUSENSE INC.·00861900000350·Coag-Sense PT/INR Meter

Assure PT Care Test Strip Kit

FDA UDI
COAGUSENSE INC.·00850040656039·Arkray Assure PT Care Test Strip, 50 Count

Coag-sense

FDA UDI
COAGUSENSE INC.·00861900000343·Coag-Sense Professional Control Test Strip Kit ...

Coag-Sense

FDA UDI
COAGUSENSE INC.·00861900000305·Coag-Sense PT/INR Meter

Coag-Sense PT/INR Professional System

FDA UDI
COAGUSENSE INC.·00861900000374·Coag-Sense PT/INR Professional System

Coag-sense

FDA UDI
COAGUSENSE INC.·00860007370878·Coag-Sense PT/INR Professional 5-Box Promo

Coag-sense

FDA UDI
COAGUSENSE INC.·00861900000312·Coag-Sense PT/INR Professional System

Coag-sense

FDA UDI
COAGUSENSE INC.·00861900000329·Coag-Sense PT/INR Patient Self-Test System

Coag-sense

FDA UDI
COAGUSENSE INC.·00860007370861·Coag-Sense PT/INR Professional 3-Box Promo

Assure PT Care PT/INR Monitoring System

FDA UDI
COAGUSENSE INC.·00850040656022·Assure PT Care PT/INR Monitoring System

Coag-Sense Test Strip Kit, 50 ct.

FDA UDI
COAGUSENSE INC.·00861900000398·Test Strip Kit, 50 ct.

Coag-sense

FDA UDI
COAGUSENSE INC.·00861900000336·Coag-Sense Test Strip Kit - 50 Ct

COAG-SENSE

FDA Adverse Event
Injury ·COAGUSENSE, INC.·Product code GJS·August 31, 2023