Taiwan FDA registration b4d99eee16bac55191e5a6f7158feed3
"JSM"Manual Patient Transfer Device(Non-Sterile)
TW: "吉生"手動病患輸送裝置(未滅菌)
Registration details
- Analysis ID
- b4d99eee16bac55191e5a6f7158feed3
- License Form
- Ministry of Health Medical Device Manufacturing Registration No. 003296
Company information
- Manufacturer
- JI SHENG MEDICAL COMPANY LIMITED
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- JI SHENG MEDICAL COMPANY LIMITED
Product details
- Intended Use
- vacuum
- Product Type (Level 1)
- J General hospital and personal use equipment
- Product Type (Level 2)
- J6785 Manual Patient Conveyor
- Import Information
- Produced in Taiwan, China
Dates and status
- Registration Date
- Oct 01, 2021
- Expiry Date
- Oct 31, 2026
About this record
Access comprehensive regulatory information for "JSM"Manual Patient Transfer Device(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 b4d99eee16bac55191e5a6f7158feed3 and manufactured by JI SHENG MEDICAL COMPANY LIMITED. The authorized representative in Taiwan is JI SHENG MEDICAL COMPANY LIMITED.
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