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Shenzhen Desida Technology Co., Ltd.

ChinaFDA applicant, unverified FDA FEI 3015924074

Devices
7
Registrations
FDA
FDA recalls
0

At a glance

Counted by deviCERTS from registry records

Market reach

United States
FDA FEI

Catalogue7

Newest first, rows 1-7 of 7

Company details

FDA FEI number
3015924074
DUNS number
418625888
Address
5th Floor, Building A, Sanmin Industrial Zone, Shilongzai, Shenzhen Guangdong

Frequently asked questions

How many devices does Shenzhen Desida Technology Co., Ltd. have in the registry?

The registry currently lists 7 devices for Shenzhen Desida Technology Co., Ltd.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Shenzhen Desida Technology Co., Ltd.'s devices?

Among its 7 most recently registered devices, Shenzhen Desida Technology Co., Ltd. has devices listed in FDA 510(k) (6 devices) and FDA GUDID (1 device). A device can be listed in more than one registry, so these counts overlap.

What risk classes do Shenzhen Desida Technology Co., Ltd.'s devices fall under?

Among its 7 most recently registered devices, the classes recorded for Shenzhen Desida Technology Co., Ltd.'s devices are Class II. Each device page shows its own class and authorisation.

What are the newest devices from Shenzhen Desida Technology Co., Ltd. in the registry?

The most recently registered devices listed for Shenzhen Desida Technology Co., Ltd. include Electric Nasal Aspirator NASA606, Electric Nasal Aspirator (NASA601, NASA602, NASA603, NASA605, NASA606, NASA608, NASA610), Baby Nasal Aspirator (BN002); Baby Nasal Aspirator (BN006); Baby Nasal Aspirator (BN007); Baby Nasal Aspirator (BN008); Baby Nasal Aspirator (BN009) and Baby Nasal Aspirator (KA1006, KA1001, KA1005, NASA005, NASA006, NASA008, NASA009).

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