# SHENZHEN ANKER MEDICAL DEVICES CO., LTD.

FEI: 3046440169
Status: Active
Establishment types: Complaint File Establishment per 21 CFR 820.198; Develop Specifications But Do Not Manufacture At This Facility; Manufacture Medical Device
Owner/operator: Shenzhen Anker Medical Devices Co., Ltd. (#10096260)

Address: Room 1601, 16F, Building 1, Runzhi R&D Center, No. 5, Runfang Road, Area 70, Xingdong Community, Xin'an Sub-district, Bao'an District, Shenzhen Guangdong, 518101, CN

Mandatory US Agent: MEDRIGHT TECH INC

## Products

Total registered: 1
Top product codes: QUG
Regulation §: 874.3305


## Source

- openFDA: https://api.fda.gov/device/registrationlisting.json?search=registration.fei_number:%223046440169%22
- FDA Registration Lookup: https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRL/rl.cfm?lid=3046440169