1,338 results
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30ms
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Sources: EU EUDAMED, US FDA
Filters
Classification: FDA Class 3
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Implantable Pulse Generator, Pacemaker (Non-Crt)
FDA Pre-Market Approval
FDA Class 3
·CONTAK RENEWAL
Implantable Pulse Generator, Pacemaker (Non-Crt)
FDA Pre-Market Approval
FDA Class 3
·INSIGNIA/NEXUS, PRIZM/VITALITY & CONTAK RENEWAL FAMILIES
Aid, Surgical, Viscoelastic
FDA Pre-Market Approval
FDA Class 3
·BIOLON 1% SODIUM HYALURONATE
Acid, Hyaluronic, Intraarticular
FDA Pre-Market Approval
FDA Class 3
·EUFLEXXA
Permanent Defibrillator Electrodes
FDA Pre-Market Approval
FDA Class 3
·FINELINE II & THINLINE II
Implantable Pulse Generator, Pacemaker (Non-Crt)
FDA Pre-Market Approval
FDA Class 3
·CONTAK RENEWAL RF HEART FAILURE PULSE GENERATORS
Implantable Pulse Generator, Pacemaker (Non-Crt)
FDA Pre-Market Approval
FDA Class 3
·PRIZM FAMILY
Implantable Pulse Generator, Pacemaker (Non-Crt)
FDA Pre-Market Approval
FDA Class 3
·CONTAK RENEWAL
Pulse Generator, Permanent, Implantable
FDA Pre-Market Approval
FDA Class 3
·MEDTRONIC REVEAL PLUS INSERTABLE LOOP RECORDER (ILR) APPLICATION SOFTWARE MODEL 9809
Tissue Adhesive Internal Use
FDA Pre-Market Approval
FDA Class 3
·LIQUIFIX FIX8 Laparoscopic Hernia Mesh Fixation Device, LIQUIFIX Precision Open Hernia Mesh Fixation Device
Tissue Adhesive Internal Use
FDA Pre-Market Approval
FDA Class 3
·LIQUIFIX FIX8 Laparoscopic Hernia Mesh Fixation Device, LIQUIFIX Precision Open Hernia Mesh Fixation Device
Tissue Adhesive Internal Use
FDA Pre-Market Approval
FDA Class 3
·LIQUIFIX FIX8 Hernia Mesh Fixation (HMF) Device, LIQUIFIX Precision Open Hernia Mesh Fixation Device
Implantable Pacemaker Pulse-Generator
FDA Pre-Market Approval
FDA Class 3
·MEDTRONIC REVEAL PLUS INSERTABLE LOOP RECORDER (ILR) WITH UPDATED TO THE APPLICATION SOFTWARE (MODEL 09-9 SERIES 2.0)
ARTERIAL BLOOD GASSING MONITORING SYSTEM (ABG)
FDA 510(k)
FDA Class 3
·Cardiovascular
Agent, Absorbable Hemostatic, Non-Collagen Based
FDA Pre-Market Approval
FDA Class 3
·PerClot Polysaccharide Hemostatic System
Test, Hepatitis B (B Core, Be Antigen, Be Antibody, B Core Igm)
FDA Pre-Market Approval
FDA Class 3
·ARCHITECT CORE (LN 6L22)
Hepatitis Viral B Dna Detection
FDA Pre-Market Approval
FDA Class 3
·ABBOTT REALTIME HBV
System, Laser, Fiber Optic, Photodynamic Therapy
FDA Pre-Market Approval
FDA Class 3
·Optiguide Cylindrical Fiber Optic
Test, Hepatitis B (B Core, Be Antigen, Be Antibody, B Core Igm)
FDA Pre-Market Approval
FDA Class 3
·ARCHITECT AUSAB, Alinity i Anti-HBs
Test, Hepatitis B (B Core, Be Antigen, Be Antibody, B Core Igm)
FDA Pre-Market Approval
FDA Class 3
·ABBOTT ARCHITECT CORE-M REAGENT KIT/CALIBRATORS/CONTROLS