Taiwan FDA registration d00c38c074269fc8556b9c4d1d48cc11
"Sakima P&O" Limb Orthosis (Non-Sterile)
TW: "佐喜真義肢" 肢體裝具 (未滅菌)
Registration details
- Analysis ID
- d00c38c074269fc8556b9c4d1d48cc11
- License Form
- Ministry of Health Medical Device Import No. 020868
- Customs Code
- DHA09402086802
Company information
- Manufacturer
- SAKIMA PROSTHETICS AND ORTHOTICS CO., LTD.
- Manufacturer Country
- Japan
- Authorized Representative
- CHENG CHUAN P&O CO., LTD.
Product details
- Product Type (Level 1)
- o Equipment for physical medicine
- Product Type (Level 2)
- O3475 Body Equipment
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Sep 17, 2019
- Expiry Date
- Sep 17, 2024
Cancellation information
- Status
- Logged out
- Reason
- 轉為登錄字號
About this record
Access comprehensive regulatory information for "Sakima P&O" Limb Orthosis (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 d00c38c074269fc8556b9c4d1d48cc11 and manufactured by SAKIMA PROSTHETICS AND ORTHOTICS CO., LTD.. The authorized representative in Taiwan is CHENG CHUAN P&O 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