21 results
·
45ms
·
Sources: EU EUDAMED, US FDA
MAJ-2370
FDA registration
SHIRAKAWA OLYMPUS CO., LTD.·2 products·🇯🇵 Japan
MAJ-2370
FDA registration
OLYMPUS MEDICAL SYSTEMS CORP.·2 products·🇯🇵 Japan
SYSTEMS INTEGRATION ENDOALPHA MEDICAL CONTROL UNIT FOR ENDOSURGERY UCES-4 Software Version 1
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
PRO-SYS
FDA UDI
BENCO DENTAL SUPPLY CO.·00366975055231·
SteriLance Impress safety lancet 26G 1.8mm
FDA UDI
Sterilance Medical (Suzhou) Inc.·16945630123310·
HUMIDIFIER, RESPIRATORY GAS
FDA registration
CBR ENTERPRISE LIMITED·1 product·🇭🇰 Hong Kong
UST-5310
FDA registration
TOCHIGI SEIKO CO., LTD·1 product·🇯🇵 Japan
Disp. humi.chamber f.F&P MR850
FDA registration
GaleMed (Xiamen) Co., Ltd.·1 product·🇨🇳 China
VentStar Heated/ Infinity ID Breathing Circuit Heated
FDA registration
VINCENT MEDICAL (DONG GUAN) MANUFACTURING CO., LTD.·1 product·🇨🇳 China
UST-5310 and UST-5311 Prosound Alpha 7, ARIETTA 70
FDA registration
FUJIFILM Corporation Medical Systems Research & Development Center Kokubunji·1 product·🇯🇵 Japan
VentStar Heated
FDA registration
Draegerwerk AG & Co. KGaA·1 product·🇩🇪 Germany
UST-5311-TIP
FDA registration
JAPAN GAS COMPANY LIMITED·1 product·🇯🇵 Japan
UST-5310 and UST-5311 Prosound Alpha 7, ARIETTA 70
FDA registration
FUJIFILM Healthcare Manufacturing Corporation Kashiwa Office·1 product·🇯🇵 Japan
PCN / Immunoglobulin G kappa heavy and light chain combined PCO / Immunoglobulin G lambda heavy and light chain combined
FDA registration
MONOCENT INC.·2 products·🇺🇸 United States
PANTHER Cutter Stapler
FDA registration
B.J.ZH.F.PANTHER MEDICAL EQUIPMENT CO.,LTD·2 products·🇨🇳 China
Endoform Antimicrobial Restorative Bioscaffold
FDA registration
Aroa Biosurgery Ltd·1 product·🇳🇿 New Zealand
TWIN-PASS OTW CATHETER, MODEL 5201
FDA 510(k)
FDA Class 2
·Cardiovascular
VENTSTAR HEATED, INFINITY ID BREATHING CIRCUIT HEATED
FDA 510(k)
FDA Class 2
·Anesthesiology
Laparoscope, General & Plastic Surgery
FDA classification
FDA Class 2
·Laparoscope, General & Plastic Surgery
Humidifier, Respiratory Gas, (Direct Patient Interface)
FDA classification
FDA Class 2
·Humidifier, Respiratory Gas, (Direct Patient Interface)