Taiwan FDA registration 288b00e4deb523858b448d9a23bbf36c
"Chentian" funnel chest correction plate system
TW: “宸田”漏斗胸矯正板系統
Taiwan·Risk Class 2·MICROWARE PRECISION CO., LTD.·Registered Mar 31, 2017 – Mar 31, 2027ActiveRegistration details
- Analysis ID
- 288b00e4deb523858b448d9a23bbf36c
Company information
- Manufacturer
- MICROWARE PRECISION CO., LTD.
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- Chentian Enterprises Co., Ltd
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- N Orthopedics
- Product Type (Level 2)
- N.3030 Single or multiple metallic bone fixation devices and accessories
- Import Information
- Contract manufacturing;; Domestic
Dates and status
- Registration Date
- Mar 31, 2017
- Expiry Date
- Mar 31, 2027
About this record
Access comprehensive regulatory information for "Chentian" funnel chest correction plate system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 288b00e4deb523858b448d9a23bbf36c and manufactured by MICROWARE PRECISION CO., LTD.. The authorized representative in Taiwan is Chentian Enterprises 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.
Free DatabasePowered by Pure Global AI89,000+ Devices