Shenzhen Bestman Instrument Co L T D

FDA Filings

This page includes the latest FDA filings for Shenzhen Bestman Instrument Co L T D. Currently, you will find the latest 100 filings for Premarket Notifications, Premarket Applications, De Novo Applications, and GUDID registrations.

FDA Registration(s)
Registration Number3008756262
FEI Number3008756262
NameSHENZHEN BESTMAN INSTRUMENT CO.,LTD
Owner & OperatorShenzhen Bestman Instrument CO.,Ltd
Contact Address4/F Block 210 2nd Nanyou Industrial Area
Shenzhen CN-44 Guangdong 518054 CN
Official Correspondent
  • Jianxing Liu
  • 086-755-26411423-x
US Agent
Registration Status1
Initial ImporterN
Registration Expiration2020-04-25
Registration Address4/F Block 210 2nd Nanyou Industrial Area
Shenzhen Guangdong, 518054 CN
Establishment TypeManufacture Medical Device

FDA Filings

Device
Company
DeviceDate
SHENZHEN BESTMAN INSTRUMENT CO.,LTD
Trade/Device name:Doppler fetal heartbeat detector2010-12-29
SHENZHEN BESTMAN INSTRUMENT CO.,LTD
Models:BF-500B,BF-500+,and BF-500++2010-12-29
SHENZHEN BESTMAN INSTRUMENT CO., LTD.
DOPPLER FETAL HEARTBEAT RATE DETECTOR2010-04-29

Related Finance Registrations
U.S. Import Records [external site]
Import IDShipmentCargo DescriptionQuantity
201902081862Hong Kong,Hong Kong -> Long Beach, CaliforniaVASCULAR DOPPLER 8MHZBV-520 (MEDICAL EQUIPMEN SCREEN / DOPPLER BF500-C C/ PANTALLA (MEDICAL EQUIPMENT) DOPPLER BF-500+ W/SCREEN / D45 CTN
2019010356841Hong Kong,Hong Kong -> Long Beach, CaliforniaVASCULAR DOPPLER 8MHZBV-520 (MEDICAL EQUIPMEN SCREEN / DOPPLER BF500-C C/ PANTALLA (MEDICAL EQUIPMENT) DOPPLER BF-500+ W/SCREEN / D45 CTN
© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.