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Medical equipment and related accessories, software and consumables
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Bioimaging and radiotherapy instruments
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Echography instruments
Echography instruments
Z1104
6,492 devices
Subcategories
3
Z110401
Ultrasound scanners
4,553
devices
›
Z110402
Ultrasound probes
1,650
devices
›
Z110490
Various ultrasound instruments
289
devices
›
Devices
Ultrasound Diagnostic System
Focus&Fusion Healthcare (Hangzhou) Co., Ltd
·
,
China
Class IIa
CE/MDR
Vinno
Vinno Technology (Suzhou) Co., Ltd
·
,
China
Class IIa
CE/MDR
Diagnostic Ultrasound System
Shenzhen Mindray Bio-Medical Electronics Co., Ltd.
·
,
China
Class IIa
CE/MDR
GUDID
on market
Diagnostic Ultrasound System
Shenzhen Mindray Bio-Medical Electronics Co., Ltd.
·
,
China
Class IIa
FDA 510(k)
K250110
Active
Cleared 16 May 2025
CE/MDR
+1
authorizations
S10
Sonoscape Medical Corp.
·
,
China
Class IIa
CE/MDR
Vinno
Vinno Technology (Suzhou) Co., Ltd
·
,
China
Class IIa
CE/MDR
BenQ
Qisda Corporation
·
,
Taiwan
Class IIa
CE/MDR
SonoSite Edge II
Fujifilm Sonosite, Inc.
·
,
United States
Class IIa
CE/MDR
X5 Exp
Sonoscape Medical Corp.
·
,
China
Class IIa
CE/MDR
GUDID
on market
BenQ
Qisda Corporation
·
,
Taiwan
Class IIa
CE/MDR
Clarius Charger HD3
Clarius Mobile Health Corp.
·
,
Canada
Class I
CE/MDR
GUDID
on market
SonoSite Edge II
Fujifilm Sonosite, Inc.
·
,
United States
Class IIa
CE/MDD
GUDID
on market
SonoSite SII
Fujifilm Sonosite, Inc.
·
,
United States
Class IIa
CE/MDD
GUDID
on market
SU11C Exp
Sonoscape Medical Corp.
·
,
China
Class IIa
CE/MDR
GUDID
on market
Ultrasound Scanners
Focus&Fusion Healthcare (Hangzhou) Co., Ltd
·
,
China
Class IIa
CE/MDR
Logiq
GE Medical Systems CO. Ltd
·
,
China
Class IIa
FDA 510(k)
K091374
Active
Cleared 26 May 2009
CE/MDR
+1
authorizations
SonoSite X-Porte
Fujifilm Sonosite, Inc.
·
,
United States
Class IIa
CE/MDD
GUDID
on market
Ultrasound Scanners
Focus&Fusion Healthcare (Hangzhou) Co., Ltd
·
,
China
Class IIa
CE/MDR
X11T
Sonoscape Medical Corp.
·
,
China
Class IIa
CE/MDR
GUDID
on market
Minisono C1-6
Alpinion Medical Systems Co., Ltd.
·
,
South Korea
Class IIa
FDA 510(k)
K182845
Active
Cleared 27 Dec 2018
CE/MDR
+1
authorizations
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