Taiwan FDA registration 84289fd08d3b7169dcf016aa482e81ba
"Difu" Solusi system
TW: "帝富" 索露西系統
Registration details
- Analysis ID
- 84289fd08d3b7169dcf016aa482e81ba
- Customs Code
- DHA00600929307
Company information
- Manufacturer
- DEPUY ORTHOPAEDICS,INC.
- Manufacturer Country
- United States
- Authorized Representative
- JOHNSON & JOHNSON MEDICAL TAIWAN LTD.
Product details
- Product Type (Level 1)
- 0399 Other artificial function substitutes
- Import Information
- import
Dates and status
- Registration Date
- Sep 02, 1999
- Expiry Date
- Sep 14, 2023
- Cancellation Date
- Sep 23, 2021
Cancellation information
- Status
- Logged out
- Reason
- 自請註銷
About this record
Access comprehensive regulatory information for "Difu" Solusi system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 84289fd08d3b7169dcf016aa482e81ba and manufactured by DEPUY ORTHOPAEDICS,INC.. The authorized representative in Taiwan is JOHNSON & JOHNSON MEDICAL TAIWAN 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