Taiwan FDA registration d284e74b778fe8a36092cffa0ae7c172
SENTEQ Limb orthosis (non-sterile)
TW: 登康美 肢體裝具 (未滅菌)
Taiwan·Risk Class 1·MD·SENTEQ CO., LTD.·Registered Dec 30, 2016 – Dec 30, 2021CancelledRegistration details
- Analysis ID
- d284e74b778fe8a36092cffa0ae7c172
- License Form
- Ministry of Health Medical Device Manufacturing No. 006545
Company information
- Manufacturer
- SENTEQ CO., LTD.
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- SENTEQ CO., LTD.
Product details
- Product Type (Level 1)
- o Equipment for physical medicine
- Product Type (Level 2)
- O3475 Body Equipment
- Import Information
- Produced in Taiwan, China
Dates and status
- Registration Date
- Dec 30, 2016
- Expiry Date
- Dec 30, 2021
Cancellation information
- Status
- Logged out
- Reason
- 轉為登錄字號
About this record
Access comprehensive regulatory information for SENTEQ Limb orthosis (non-sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number d284e74b778fe8a36092cffa0ae7c172 and manufactured by SENTEQ CO., LTD.. The authorized representative in Taiwan is SENTEQ 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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