Taiwan FDA registration 5217da48aef7bd75ba988d218bd4d762
"Keystone" Mizzy Articulating Paper (Non-Sterile)
TW: "啟史東" 咬合紙 (未滅菌)
Registration details
- Analysis ID
- 5217da48aef7bd75ba988d218bd4d762
- License Form
- Ministry of Health Medical Device Import Registration No. 003471
- Customs Code
- DHA08400347105
Company information
- Manufacturer
- KEYSTONE INDUSTRIES
- Manufacturer Country
- United States
- Authorized Representative
- TUNG SHENG INTERNATIONAL INC.
Product details
- Intended Use
- Limited to the first plastic grade identification range of the Measures for the Administration of Medical Devices (occlusal paper [F.6140]).
- Product Type (Level 1)
- F Dental devices
- Product Type (Level 2)
- F6140 Occlusal paper
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Oct 01, 2021
- Expiry Date
- Oct 31, 2026
About this record
Access comprehensive regulatory information for "Keystone" Mizzy Articulating Paper (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 5217da48aef7bd75ba988d218bd4d762 and manufactured by KEYSTONE INDUSTRIES. The authorized representative in Taiwan is TUNG SHENG INTERNATIONAL INC..
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