Taiwan FDA registration e1b2189f7a71699e7d7cbc05ceb1abc6
"Paili" alternating pressure air mattress (unsterilized)
TW: “派立” 交替式壓力氣墊床(未滅菌)
Taiwan·Risk Class 1·RONDON INDUSTRIES LIMITED·Registered Jan 20, 2011 – Jan 20, 2026ExpiredRegistration details
- Analysis ID
- e1b2189f7a71699e7d7cbc05ceb1abc6
- Customs Code
- DHA04400982903
Company information
- Manufacturer
- RONDON INDUSTRIES LIMITED
- Manufacturer Country
- Hong Kong
- Authorized Representative
- PE & LE ENTERPRISE LTD.
Product details
- Intended Use
- Limited to the classification and grading management method of medical equipment "Alternating pressure air mattress (J.5550)" level identification range.
- Product Type (Level 1)
- J General hospital and personal use equipment
- Product Type (Level 2)
- J.5550 交替式壓力氣墊床
- Import Information
- import
Dates and status
- Registration Date
- Jan 20, 2011
- Expiry Date
- Jan 20, 2026
About this record
Access comprehensive regulatory information for "Paili" alternating pressure air mattress (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number e1b2189f7a71699e7d7cbc05ceb1abc6 and manufactured by RONDON INDUSTRIES LIMITED. The authorized representative in Taiwan is PE & LE ENTERPRISE 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