Taiwan FDA registration 9395c039e28c2d95531fbd3071a94fee
“CSI” Alternating Pressure Air Flotation Mattress(Non-Sterile)
TW: “繁葵”交替式壓力氣墊床(未滅菌)
Taiwan·Risk Class 1·MD·CAREMED SUPPLY INC.·Registered Sep 26, 2018 – Sep 26, 2028ActiveRegistration details
- Analysis ID
- 9395c039e28c2d95531fbd3071a94fee
- License Form
- Ministry of Health Medical Device Manufacturing No. 007452
Company information
- Manufacturer
- CAREMED SUPPLY INC.
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- CAREMED SUPPLY INC.
Product details
- Intended Use
- Limited to the first level identification range of the Measures for the Administration of Medical Equipment "Alternating Pressure Air Mattress (J.5550)".
- Product Type (Level 1)
- J General hospital and personal use equipment
- Product Type (Level 2)
- J5550 Alternating pressure air mattress
- Import Information
- Produced in Taiwan, China
Dates and status
- Registration Date
- Sep 26, 2018
- Expiry Date
- Sep 26, 2028
About this record
Access comprehensive regulatory information for “CSI” Alternating Pressure Air Flotation Mattress(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 9395c039e28c2d95531fbd3071a94fee and manufactured by CAREMED SUPPLY INC.. The authorized representative in Taiwan is CAREMED SUPPLY INC..
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