Taiwan FDA registration 38ec617fb8df8d27f2b7dc4c5f9f0451
"Global Allianz" titanium membrane system
TW: “全球安聯”鈦膜系統
Taiwan·Risk Class 2·ALLIANCE GLOBAL TECHNOLOGY CO., LTD.·Registered Nov 30, 2017 – Nov 30, 2027ActiveRegistration details
- Analysis ID
- 38ec617fb8df8d27f2b7dc4c5f9f0451
Company information
- Manufacturer
- ALLIANCE GLOBAL TECHNOLOGY CO., LTD.
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- ALLIANCE GLOBAL TECHNOLOGY CO., LTD.
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- F Dentistry
- Product Type (Level 2)
- F.4760 骨板;; F.4880 骨內固定螺釘或金屬線
- Import Information
- Domestic
Dates and status
- Registration Date
- Nov 30, 2017
- Expiry Date
- Nov 30, 2027
About this record
Access comprehensive regulatory information for "Global Allianz" titanium membrane system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 38ec617fb8df8d27f2b7dc4c5f9f0451 and manufactured by ALLIANCE GLOBAL TECHNOLOGY CO., LTD.. The authorized representative in Taiwan is ALLIANCE GLOBAL TECHNOLOGY 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