Taiwan FDA registration e3e22c6129fef52ce88a4bcf90be8640
"Difu" Kangfu vertebral cement system
TW: “帝富”康富脊椎骨水泥系統
Registration details
- Analysis ID
- e3e22c6129fef52ce88a4bcf90be8640
- Customs Code
- DHA05602822401
Company information
- Manufacturer Country
- Switzerland
- Authorized Representative
- JOHNSON & JOHNSON MEDICAL TAIWAN LTD.
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- N Orthopedics
- Product Type (Level 2)
- N.3027 PMMA骨水泥
- Import Information
- Input;; Contract manufacturing
Dates and status
- Registration Date
- Mar 11, 2016
- Expiry Date
- Mar 11, 2026
About this record
Access comprehensive regulatory information for "Difu" Kangfu vertebral cement system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number e3e22c6129fef52ce88a4bcf90be8640 and manufactured by MEDOS INTERNATIONAL SARL;; Jabil Switzerland Manufacturing GmbH. 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