Taiwan FDA registration da06767e1a2d9a7a8cc04a9ece3bf78a
“PE&LE ENTERPRISE” Alternating pressure air flotation mattress (Non-sterile)
TW: “派立” 交替式壓力氣墊床(未滅菌)
Taiwan·Risk Class 1·MD·PE & LE ENTERPRISE LTD.·Registered Jun 28, 2019 – Jun 28, 2024ExpiredRegistration details
- Analysis ID
- da06767e1a2d9a7a8cc04a9ece3bf78a
- License Form
- Ministry of Health Medical Device Manufacturing No. 007825
Company information
- Manufacturer
- PE & LE ENTERPRISE LTD.
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- PE & LE ENTERPRISE LTD.
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
- Jun 28, 2019
- Expiry Date
- Jun 28, 2024
About this record
Access comprehensive regulatory information for “PE&LE ENTERPRISE” 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 da06767e1a2d9a7a8cc04a9ece3bf78a and manufactured by PE & LE ENTERPRISE LTD.. The authorized representative in Taiwan is PE & LE ENTERPRISE LTD..
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