3,416 results · 45ms · Sources: EU EUDAMED, US FDA

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N-Histofine DAB-3S KIT

Device
EU IVDR · Eu Ivd Class A ·Nichirei Biosciences Inc.·On the market·10 countries

N-Histofine DAB-3S KIT

Device
EU IVDR · Eu Ivd Class A ·Nichirei Biosciences Inc.·On the market·10 countries

N-Histofine DAB-3S KIT

Device
EU IVDR · Eu Ivd Class A ·Nichirei Biosciences Inc.·On the market·10 countries

PolyQ Stain DAB Substrate Buffer

Device
EU IVDR · Eu Ivd Class A ·biocyc Biotechnologie GmbH & Co. KG·On the market

PolyQ Stain DAB Substrate Buffer

Device
EU IVDR · Eu Ivd Class A ·biocyc Biotechnologie GmbH & Co. KG·On the market

PolyQ Stain DAB Substrate Buffer

Device
EU IVDR · Eu Ivd Class A ·biocyc Biotechnologie GmbH & Co. KG·On the market

PolyQ Stain DAB Substrate Buffer

Device
EU IVDR · Eu Ivd Class A ·biocyc Biotechnologie GmbH & Co. KG·On the market

PolyQ Stain DAB Substrate Buffer

Device
EU IVDR · Eu Ivd Class A ·biocyc Biotechnologie GmbH & Co. KG·On the market

ODS Surgical Guide

FDA registration
ODS CO., LTD.·1 product·🇰🇷 South Korea

ODS Clear Resin - Retainer

FDA registration
ODS CO., LTD.·1 product·🇰🇷 South Korea

Scan Cure (SC-80)

FDA registration
ODS CO., LTD.·1 product·🇰🇷 South Korea

Drug-Coated Peripheral Transluminal Angioplasty Catheter

FDA Pre-Market Approval
FDA Class 3 ·Lutonix 018 Drug Coated Balloon PTA Catheter (Lutonix DCB)

Drug-Eluting Peripheral Transluminal Angioplasty Catheter

FDA Pre-Market Approval
FDA Class 3 ·Lutonix 035 Drug Coated Balloon PTA Catheter (Lutonix DCB)

Drug-Eluting Peripheral Transluminal Angioplasty Catheter

FDA Pre-Market Approval
FDA Class 3 ·Lutonix 018 Drug Coated Balloon PTA Catheter (Lutonix DCB)

Drug-Eluting Peripheral Transluminal Angioplasty Catheter

FDA Pre-Market Approval
FDA Class 3 ·Lutonix 035 Drug Coated Balloon PTA Catheter (Lutonix DCB)

Drug-Eluting Peripheral Transluminal Angioplasty Catheter

FDA Pre-Market Approval
FDA Class 3 ·Lutonix 035 Drug Coated Balloon PTA Catheter (Lutonix DCB)

System, Test, Her-2/Neu, Ihc

FDA Pre-Market Approval
FDA Class 3 ·PATHWAY ANTI-HER-2/NEU (4B5) RABBIT MONOCLONAL PRIMARY ANTIBODY

Immunohistochemistry Antibody Assay, C-Kit

FDA Pre-Market Approval
FDA Class 3 ·PATHWAY ANTI-C-KIT (9.7) PRIMARY ANTIBODY

COBAS INTEGRA SYSTEM

FDA registration
ROCHE DIAGNOSTICS GMBH·62 products·🇩🇪 Germany

COBAS INTEGRA SYSTEM

FDA registration
ROCHE DIAGNOSTICS INTERNATIONAL LTD.·62 products·🇨🇭 Switzerland