Astrasono Technology Co., Ltd.
ChinaFDA 510(k) applicant, unverified FDA FEI 3042254626
- Devices
- 5
- Registrations
- FDA
- FDA recalls
- 0
At a glance
Market reach
- United States
- FDA FEI
What Astrasono Technology Co., Ltd. makes
Astrasono Technology Co., Ltd. manufactures the Astrasono A3Pro Bladder Scanner, a medical device used for bladder scanning purposes.
The Astrasono A3Pro Bladder Scanner is classified as a Class II medical device and is listed in the FDA 510(k) registry. The company is based in the US.
Catalogue
- GUDID
- GUDID
- GUDID
- GUDID
Astrasono A3Pro Bladder Scanner (A3Pro) Ref K250331
510(k) 510(k)
Company details
- FDA FEI number
- 3042254626
- DUNS number
- 449989331
- Address
- 805B, Nangang Business Building, 1428 Qianhai Rd, Xiangnan Community, Nanshan Subdistrict, Nanshan, Shenzhen Guangdong
Frequently asked questions
How many devices does Astrasono Technology Co., Ltd. have in the registry?
The registry currently lists 5 devices for Astrasono Technology Co., Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Astrasono Technology Co., Ltd.'s devices?
Among its 5 most recently registered devices, Astrasono Technology Co., Ltd. has devices listed in FDA 510(k) (1 device) and FDA GUDID (4 devices). A device can be listed in more than one registry, so these counts overlap.
What risk classes do Astrasono Technology Co., Ltd.'s devices fall under?
Among its 5 most recently registered devices, the classes recorded for Astrasono Technology Co., Ltd.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Astrasono Technology Co., Ltd. in the registry?
The most recently registered devices listed for Astrasono Technology Co., Ltd. include Astrasono A3Pro Bladder Scanner, Astrasono A3Pro Lite Bladder Scanner, Astrasono A5Pro Bladder Scanner and Astrasono A3Essential Bladder Scanner.