Taiwan FDA registration 518761badfeaceefc9fad6223c587755
“Bausch”Articulation Paper (Non-Sterile)
TW: “博斯”咬合紙(未滅菌)
Taiwan·Risk Class 1·MD·DR. JEAN BAUSCH KG·Registered Oct 01, 2021 – Oct 31, 2026ActiveRegistration details
- Analysis ID
- 518761badfeaceefc9fad6223c587755
- License Form
- Ministry of Health Medical Device Import Registration No. 009701
- Customs Code
- DHA08400970100
Company information
- Manufacturer
- DR. JEAN BAUSCH KG
- Manufacturer Country
- Germany
- 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 “Bausch”Articulation 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 518761badfeaceefc9fad6223c587755 and manufactured by DR. JEAN BAUSCH KG. 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