Taiwan FDA registration 59100d40b6d2cf51348dae01f2b0ffb7
"Difu" Ressis artificial knee joint
TW: "帝富" 雷西士人工膝關節
Taiwan·Risk Class 2·DEPUY ORTHOPAEDICS,INC.·Registered Nov 16, 2000 – Nov 16, 2015CancelledRegistration details
- Analysis ID
- 59100d40b6d2cf51348dae01f2b0ffb7
- Customs Code
- DHA00600955702
Company information
- Manufacturer
- DEPUY ORTHOPAEDICS,INC.
- Manufacturer Country
- United States
- Authorized Representative
- JOHNSON & JOHNSON MEDICAL TAIWAN LTD.
Product details
- Product Type (Level 1)
- N000 Orthopedics
- Import Information
- import
Dates and status
- Registration Date
- Nov 16, 2000
- Expiry Date
- Nov 16, 2015
- Cancellation Date
- Apr 25, 2018
Cancellation information
- Status
- Logged out
- Reason
- 自行鍵入
About this record
Access comprehensive regulatory information for "Difu" Ressis artificial knee joint in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 59100d40b6d2cf51348dae01f2b0ffb7 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