507 results
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33ms
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Sources: EU EUDAMED, US FDA
MULTIPLE A-C POWERED
FDA registration
Teleflex LLC (NADC)·1 product·🇺🇸 United States
QP Medtech International AB
Manufacturer
🇸🇪 Sweden
QiVi Male External Urine Management Device
FDA registration
QNQ Design and Development Pvt. Ltd.·1 product·🇮🇳 India
Qora Collection Bags
FDA registration
QNQ Design and Development Pvt. Ltd.·1 product·🇮🇳 India
QiVi Lite Male External Urine Management Device
FDA registration
QNQ Design and Development Pvt. Ltd.·1 product·🇮🇳 India
Qoramatic, Qoramatic Drainage Bags
FDA registration
QNQ Design and Development Pvt. Ltd.·1 product·🇮🇳 India
Qora Aeon Stool Management Kit
FDA registration
QNQ Design and Development Pvt. Ltd.·1 product·🇮🇳 India
Pulse Generator, Pacemaker, Implantable, With Cardiac Resynchronization (Crt-P)
FDA Pre-Market Approval
FDA Class 3
·Sentus ProMRI OTW QP S-75, Sentus ProMRI OTW QP S-85, Sentus ProMRI OTW QP S-95, Sentus ProMRI OTW QP L-75, Sentus ProMR
Pulse Generator, Pacemaker, Implantable, With Cardiac Resynchronization (Crt-P)
FDA Pre-Market Approval
FDA Class 3
·Sentus ProMRI OTW QP S-75, Sentus ProMRI OTW QP S-85, Sentus ProMRI OTW QP S-95, Sentus ProMRI OTW QP L-75, Sentus ProMR
Pulse Generator, Pacemaker, Implantable, With Cardiac Resynchronization (Crt-P)
FDA Pre-Market Approval
FDA Class 3
·Sentus ProMRI OTW QP S-75, Sentus ProMRI OTW QP S-85, Sentus ProMRI OTW QP S-95, Sentus ProMRI OTW QP L-75, Sentus ProMR
Pulse Generator, Pacemaker, Implantable, With Cardiac Resynchronization (Crt-P)
FDA Pre-Market Approval
FDA Class 3
·Sentus ProMRI OTW QP S-75, Sentus ProMRI OTW QP S-85, Sentus ProMRI OTW QP S-95, Sentus ProMRI OTW QP L-75, Sentus ProMR
Pulse Generator, Pacemaker, Implantable, With Cardiac Resynchronization (Crt-P)
FDA Pre-Market Approval
FDA Class 3
·Sentus ProMRI OTW QP S-75, Sentus ProMRI OTW QP S-85, Sentus ProMRI OTW QP S-95, Sentus ProMRI OTW QP L-75, Sentus ProMR
Macroplastique Implants
FDA UDI
Uroplasty, Inc.·08717591240266·Soft tissue bulking agent indicated for transur...
SURGICAL INSTRUMENT
FDA UDI
Sin Sistema de Implante Nacional S/A·07899995205476·PROSTHETIC DRUM
QTQ / Reagents, non-variola Orthopoxvirus nucleic acid.
FDA registration
MONOCENT INC.·1 product·🇺🇸 United States
Pulse Generator, Pacemaker, Implantable, With Cardiac Resynchronization (Crt-P)
FDA Pre-Market Approval
FDA Class 3
·Sentus ProMRI OTW QP S, Sentus ProMRI OTW QP S-xx/49, Sentus ProMRI OTW QP L, Sentus ProMRI OTW QP Lxx/49m, Evia HF, Evi
MPQ-42
FDA 510(k)
FDA Class 2
·Radiology
IsoLED Ac=Powered LED Headlight System
FDA registration
Medical Illumination International, Inc·2 products·🇺🇸 United States
VISTA HPQ SYSTEM
FDA 510(k)
FDA Class 2
·Radiology
VISTA HPQ SYSTEM
FDA 510(k)
FDA Class 2
·Radiology