5,690 results
·
40ms
·
Sources: EU EUDAMED, US FDA
Colibrí™
FDA UDI
COPAN WASP SRL·58050148218208·Colibrí™
Colibrí™ Primary Tube for VITEK 2
FDA UDI
COPAN WASP SRL·18050148217968·Colibrí™ Primary Tube for VITEK 2
Visby Medical Women's Sexual Health Test
FDA 510(k)
FDA Class 2
·Microbiology
TendoNova Ocelot
FDA UDI
Tendonova Corporation·00860009899827·TendoNova Disposable Unit 80mm Kit
Colibrí
FDA 510(k)
FDA Class 2
·Microbiology
DermaSensor
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
BD Kiestra IdentifA
FDA 510(k)
FDA Class 2
·Microbiology
BD Kiestra IdentifA
FDA 510(k)
FDA Class 2
·Microbiology
Colibri System
FDA 510(k)
FDA Class 2
·Microbiology
Spray do nosa
Basic UDI-DI
EU MDD
·
Eu Md Class 1
·GLOBAL PHARMA CM S.A·1 device
Implantable Transprostatic Tissue Retractor System
FDA classification
FDA Class 2
·Implantable Transprostatic Tissue Retractor System
HD 2062692-1
Certificate
MDD Annex II (excluding section 4)·Nexmed Technology Co.,Ltd.·TÜV Rheinland LGA Products GmbH·6 Basic UDI-DIs
HD 2062682-1
Certificate
MDD Annex II (excluding section 4)·Nexmed Technology Co.,Ltd.·TÜV SÜD Product Service GmbH·1 Basic UDI-DI
BYO-TECH SAS
Authorized representative
🇫🇷 France·1 Manufacturer·11 Devices
Temporarily-Placed Urethral Opening System For Symptoms Of Benign Prostatic Hyperplasia
FDA classification
FDA Class 2
·Temporarily-Placed Urethral Opening System For Symptoms Of Benign Prostatic Hyperplasia
Agents, Embolic, For Treatment Of Benign Prostatic Hyperplasia
FDA classification
FDA Class 2
·Agents, Embolic, For Treatment Of Benign Prostatic Hyperplasia
Respirator, N95, For Use By The General Public In Public Health Medical Emergencies
FDA classification
FDA Class 2
·Respirator, N95, For Use By The General Public In Public Health Medical Emergencies
EH-CSB-A,EH-CSB-B,EH-CSB-C,EH-CSB-D,EH-CSB-E,EH-CSB-F,EH-CSB-G
Basic UDI-DI
EU MDR
·
Eu Md Class 1
·Tianjin Enou-health Medical Device Tech Co.,Ltd·1 device
Scarmed Silicon Gel & Scarmed Plus Gel
Basic UDI-DI
EU MDR
·
Eu Md Class 1
·Sana Pharmaceutical Industry marketed by Sana Pharmaceutical Research Company·1 device
Forceps, Biopsy, Bronchoscope (Non-Rigid)
FDA classification
FDA Class 2
·Forceps, Biopsy, Bronchoscope (Non-Rigid)