Taiwan FDA registration b99b908facbf1dd4cbea97ae4a05534c
Metrarathi Line
TW: 美特拉拉提線
Registration details
- Analysis ID
- b99b908facbf1dd4cbea97ae4a05534c
Company information
- Manufacturer
- SHINEO TECHNOLOGY CO., LTD.
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- DIAMOND BIOTECHNOLOGY CO., LTD.
Product details
- Intended Use
- Details are as detailed as approved Chinese instructions
- Product Type (Level 1)
- I General, Plastic Surgery and Dermatology
- Product Type (Level 2)
- I.4840 Absorbable polydioxanone surgical joint
- Import Information
- Contract manufacturing;; Security Surveillance;; Domestic
Dates and status
- Registration Date
- Jul 19, 2023
- Expiry Date
- Jul 19, 2028
About this record
Access comprehensive regulatory information for Metrarathi Line in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number b99b908facbf1dd4cbea97ae4a05534c and manufactured by SHINEO TECHNOLOGY CO., LTD.. The authorized representative in Taiwan is DIAMOND BIOTECHNOLOGY 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