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Jiangsu Kangbao Medical Equipment Co., Ltd.

Active in EUDAMED

Chinafrom SRN EUDAMED SRN CN-MF-000025682

Devices
19
Registrations
EUDAMED

At a glance

Counted by deviCERTS from registry records

Market reach

European Union
EUDAMED actor

Catalogue19

Newest first, rows 1-19 of 19

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Rows 1-19 of 19

Company details

EUDAMED SRN
CN-MF-000025682
EUDAMED status
Active
EUDAMED registered name
Jiangsu Kangbao Medical Equipment Co., Ltd.
Registered address
78#, 78#, North Suzhong Road, Baoying, 225800, Yangzhou, China
Phone
+86-18921918521
PRRC contact
Wenbin Fan(public in EUDAMED)

Frequently asked questions

How many devices does Jiangsu Kangbao Medical Equipment Co., Ltd. have in the registry?

The registry currently lists 19 devices for Jiangsu Kangbao Medical Equipment Co., Ltd.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Jiangsu Kangbao Medical Equipment Co., Ltd.'s devices?

Among its 19 most recently registered devices, Jiangsu Kangbao Medical Equipment Co., Ltd. has devices listed in EUDAMED (15 devices) and FDA 510(k) (4 devices). A device can be listed in more than one registry, so these counts overlap.

What risk classes do Jiangsu Kangbao Medical Equipment Co., Ltd.'s devices fall under?

Among its 19 most recently registered devices, the classes recorded for Jiangsu Kangbao Medical Equipment Co., Ltd.'s devices are Class I, Class IIa and Class II. Each device page shows its own class and authorisation.

What are the newest devices from Jiangsu Kangbao Medical Equipment Co., Ltd. in the registry?

The most recently registered devices listed for Jiangsu Kangbao Medical Equipment Co., Ltd. include Sterile Hypodermic Needle for Single Use, Sterile Enteral syringe, Safety scalp vein set, Scalp vein set, Blood collection needle (Scalp vein set type), Blood collection needle (Needle holder type), Safety blood collection needle (Scalp vein set type), Safety blood collection needle (Needle holder type) and Sterile Hypodermic Syringes for single use.

Generated automatically from registry data and not verified by a human reviewer.