Taiwan FDA registration d26b1ef8c010f1eada75375360dccfd4
“Syntellix” Magnezix CS
TW: “信德立”可吸收鎂合金骨螺釘
Registration details
- Analysis ID
- d26b1ef8c010f1eada75375360dccfd4
- License Form
- Ministry of Health Medical Device Import No. 033408
- Customs Code
- DHA05603340805
Company information
- Manufacturer
- Syntellix AG
- Manufacturer Country
- Germany
- Authorized Representative
- MEDLION BIOTECH CO., LTD.
Product details
- Intended Use
- MAGNEZIX CS bioresorbable compression screws can be used for fracture reduction fixation in specific parts, osteotomy fixation and other fracture repositioning fixation and joint fusion of specific joints. THE PURPOSE OF USING MAGNEZIX CS IS TO SURGICALLY REDUCE AND FIX BONE FRAGMENTS IN AN ANATOMICAL POSITION UNTIL THE BONE HEALS. Implants are for single use only.
- Product Type (Level 1)
- N Orthopedic devices
- Product Type (Level 2)
- N3040 Smooth or threaded metal bone fixation
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- May 05, 2020
- Expiry Date
- May 05, 2025
About this record
Access comprehensive regulatory information for “Syntellix” Magnezix CS in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number d26b1ef8c010f1eada75375360dccfd4 and manufactured by Syntellix AG. The authorized representative in Taiwan is MEDLION BIOTECH 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