Taiwan FDA registration cac07e5f70dd6309ae03a8bc1cf97395
“FORA”Automatic Blood Pressure Monitor
TW: “福爾”醫用隧道式血壓計
Taiwan·Risk Class 2·MD·Taibo Technology Co., Ltd. five-stock factory·Registered Nov 25, 2022 – Nov 25, 2027ActiveRegistration details
- Analysis ID
- cac07e5f70dd6309ae03a8bc1cf97395
- License Form
- Ministry of Health Medical Device Manufacturing No. 007774
Company information
- Manufacturer
- Taibo Technology Co., Ltd. five-stock factory
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- TAIDOC TECHNOLOGY CORPORATION
Product details
- Intended Use
- Details are as detailed as approved Chinese instructions
- Product Type (Level 1)
- E Cardiovascular Medicine Science
- Product Type (Level 2)
- E1130 Non-invasive blood pressure measurement system
- Import Information
- Produced in Taiwan, China
Dates and status
- Registration Date
- Nov 25, 2022
- Expiry Date
- Nov 25, 2027
About this record
Access comprehensive regulatory information for “FORA”Automatic 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 cac07e5f70dd6309ae03a8bc1cf97395 and manufactured by Taibo Technology Co., Ltd. five-stock factory. The authorized representative in Taiwan is TAIDOC TECHNOLOGY CORPORATION.
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