Taiwan FDA registration 2a4b5359fecd0ca5327547384254fe37
"Xinpuwei" alternating pressure air mattress (unsterilized)
TW: "鑫普威" 交替式壓力氣墊床 (未滅菌)
Taiwan·Risk Class 1·AIRFLO (XIAMEN) MEDICAL CO. LTD.·Registered Oct 25, 2012 – Oct 25, 2017CancelledRegistration details
- Analysis ID
- 2a4b5359fecd0ca5327547384254fe37
- Customs Code
- DHA04600177508
Company information
- Manufacturer
- AIRFLO (XIAMEN) MEDICAL CO. LTD.
- Manufacturer Country
- China
- Authorized Representative
- MAXHEALTH CORPORATION
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)
- J.5550 交替式壓力氣墊床
- Import Information
- Input;; Chinese goods
Dates and status
- Registration Date
- Oct 25, 2012
- Expiry Date
- Oct 25, 2017
- Cancellation Date
- Dec 20, 2019
Cancellation information
- Status
- Logged out
- Reason
- 未展延而逾期者
About this record
Access comprehensive regulatory information for "Xinpuwei" 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 2a4b5359fecd0ca5327547384254fe37 and manufactured by AIRFLO (XIAMEN) MEDICAL CO. LTD.. The authorized representative in Taiwan is MAXHEALTH CORPORATION.
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