Taiwan FDA registration f90d1661517497cb5ccf28fd6a1d01f5
SARO Limb orthosis (Non-Sterile)
TW: 莎蘿日記 肢體裝具 (未滅菌)
Taiwan·Risk Class 1·MD·LINHAI DUQIAO FENG SHAN FU QIANG GLASSES CO. LTD.·Registered Dec 17, 2021 – Oct 31, 2023ExpiredRegistration details
- Analysis ID
- f90d1661517497cb5ccf28fd6a1d01f5
- License Form
- Ministry of Health Medical Device Land Transport Registration No. a00009
- Customs Code
- DHA086a0000905
Company information
- Manufacturer Country
- China
- Authorized Representative
- DA GUAN INTERNATIONAL ELECTRONICS CO., LTD.
Product details
- Intended Use
- Limited to the first level recognition range of medical equipment classification and grading management measures limb equipment (O.3475).
- Product Type (Level 1)
- o Physical Medical Sciences
- Product Type (Level 2)
- O3475 Body Equipment
Dates and status
- Registration Date
- Dec 17, 2021
- Expiry Date
- Oct 31, 2023
About this record
Access comprehensive regulatory information for SARO 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 f90d1661517497cb5ccf28fd6a1d01f5 and manufactured by LINHAI DUQIAO FENG SHAN FU QIANG GLASSES CO. LTD.. The authorized representative in Taiwan is DA GUAN INTERNATIONAL ELECTRONICS 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