10,000 results · 49ms · Sources: EU EUDAMED, US FDA

PermaSoft

FDA registration
The Myerson Company Limited·1 product·🇹🇹 Trinidad and Tobago

Torosa

FDA UDI
Coloplast A/S·05708932470858·Saline Filled Testicular Prosthesis

Torosa

FDA UDI
Coloplast A/S·05708932470797·Saline Filled Testicular Prosthesis

Torosa

FDA UDI
Coloplast A/S·05708932470810·Saline Filled Testicular Prosthesis

Torosa

FDA UDI
Coloplast A/S·05708932470834·Saline Filled Testicular Prosthesis

EMSRUN

FDA UDI
Wuxi Emsrun Technology Co., Ltd.·06974567745305·

EMSRUN

FDA UDI
Wuxi Emsrun Technology Co., Ltd.·06974567745282·

Implantable Cardioverter Defibrillator (Non-Crt)

FDA Pre-Market Approval
FDA Class 3 ·ENDOTAK RELIANCE 4-SITE DEFIBRILLATION LEADS

Implantable Pulse Generator, Pacemaker (Non-Crt)

FDA Pre-Market Approval
FDA Class 3 ·VIGOR, MERIDIAN, DISCOVER FAMILIES OF PACEMAKER

Prosthesis, Hip, Semi-Constrained, Metal/Ceramic/Ceramic/Metal, Cemented Or Uncemented

FDA Pre-Market Approval
FDA Class 3 ·Trident Alumina Insert

Implantable Pulse Generator, Pacemaker (Non-Crt)

FDA Pre-Market Approval
FDA Class 3 ·VENTAK AV, VENTAK PRIZM, VITALITY, CONFIENT, TELIGEN, INCEPTA, ENERGEN, PUNCTUA FAMILIES OF ICDS

Implantable Pulse Generator, Pacemaker (Non-Crt)

FDA Pre-Market Approval
FDA Class 3 ·VENTAK CD, CONTAK RENEWAL, LIVIAN, COGNIS, INCEPTA, ENERGEN, PUNCTUA FAMILIES OF CRT-DS

Implantable Cardioverter Defibrillator (Non-Crt)

FDA Pre-Market Approval
FDA Class 3 ·AID-B/BR AND VENTAK ICD

Pulse Generator, Pacemaker, Implantable, With Cardiac Resynchronization (Crt-P)

FDA Pre-Market Approval
FDA Class 3 ·CONTAK RENEWAL TR, INVIVE, INTUA FAMILIES OF CRT-PS

Implantable Cardioverter Defibrillator (Non-Crt)

FDA Pre-Market Approval
FDA Class 3 ·VENTAK PRX, VENTAK MINI FAMILIES OF ICDS

Implantable Pulse Generator, Pacemaker (Non-Crt)

FDA Pre-Market Approval
FDA Class 3 ·PULSAR, PULSAR MAX, DISCOVER, INSIGNIA, ALTRUA, INGENIO, ADVANTIO, VITALIO, FORMIO FAMILIES OF PACEMAKER

Laser, Neodymium:Yag, Ophthalmic For Posterior Capsulotomy And Cutting Pupilla

FDA Pre-Market Approval
FDA Class 2 ·NEODYMIUM-YAG OP LASER OPL-3

Laser, Neodymium:Yag, Ophthalmic For Posterior Capsulotomy And Cutting Pupilla

FDA Pre-Market Approval
FDA Class 2 ·NEODYMIUM-YAG OP LASER OPL-3

Fluid, Intraocular

FDA Pre-Market Approval
FDA Class 3 ·ADATO SIL-O1 5000 SILICONE OIL

Laser, Neodymium:Yag, Ophthalmic For Posterior Capsulotomy And Cutting Pupilla

FDA Pre-Market Approval
FDA Class 2 ·NEODYMIUM-YAG OP LASER OPL-3