Taiwan FDA registration 9e9a3abb0d395794d2cde748e694a44b
"Esther" arm electronic blood pressure monitor
TW: “以斯帖”臂式電子血壓計
Registration details
- Analysis ID
- 9e9a3abb0d395794d2cde748e694a44b
- Customs Code
- DHA09200098004
Company information
- Manufacturer
- Truly Instrument Ltd.
- Manufacturer Country
- China
- Authorized Representative
- ESTI BIOMEDICAL TECHNOLOGY CORP.
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- E Cardiovascular Medicine Science
- Import Information
- Input;; Chinese goods
Dates and status
- Registration Date
- Mar 05, 2019
- Expiry Date
- Mar 05, 2024
About this record
Access comprehensive regulatory information for "Esther" arm electronic blood pressure monitor in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 9e9a3abb0d395794d2cde748e694a44b and manufactured by Truly Instrument Ltd.. The authorized representative in Taiwan is ESTI BIOMEDICAL TECHNOLOGY CORP..
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.
Free DatabasePowered by Pure Global AI89,000+ Devices