Taiwan FDA registration 0a465de79278fd84eb66ed4149173cbc
"Madebaokang" arm-type electronic sphygmomanometer
TW: "馬德保康" 手臂式電子血壓計
Registration details
- Analysis ID
- 0a465de79278fd84eb66ed4149173cbc
- Customs Code
- DHA09200159700
Company information
- Manufacturer
- Shenzhen AOJ Medical Technology Co., Ltd.
- Manufacturer Country
- China
- Authorized Representative
- HENG LEONG HANG CO., LTD.
Product details
- Intended Use
- Details are as detailed as approved Chinese instructions
- Product Type (Level 1)
- E Cardiovascular Medicine Science
- Product Type (Level 2)
- E.1130.
- Import Information
- Input;; Chinese goods
Dates and status
- Registration Date
- Sep 27, 2024
- Expiry Date
- Sep 27, 2029
About this record
Access comprehensive regulatory information for "Madebaokang" arm-type electronic sphygmomanometer in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 0a465de79278fd84eb66ed4149173cbc and manufactured by Shenzhen AOJ Medical Technology Co., Ltd.. The authorized representative in Taiwan is HENG LEONG HANG CO., LTD..
This page provides complete technical specifications, regulatory compliance details. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.
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