Taiwan FDA registration 0d0e74321f7c7bd9993e1f9052acea52
"Keystone" Mizzy dental articulating material (Non-Sterile)
TW: "基石" 易即牙科專用咬合材料 (未滅菌)
Registration details
- Analysis ID
- 0d0e74321f7c7bd9993e1f9052acea52
- License Form
- Ministry of Health Medical Device Import Registration No. 009573
- Customs Code
- DHA08400957304
Company information
- Manufacturer
- KEYSTONE INDUSTRIES
- Manufacturer Country
- United States
- Authorized Representative
- SHIN YEAN TRADING CO., LTD.
Product details
- Intended Use
- Limited to the first level recognition range of occlusal paper (F.6140) of the Measures for the Administration of Medical Equipment.
- 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 dental articulating material (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 0d0e74321f7c7bd9993e1f9052acea52 and manufactured by KEYSTONE INDUSTRIES. The authorized representative in Taiwan is SHIN YEAN TRADING 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