Taiwan FDA registration f627aa773ad3fbb30b43c4de993304fe
"Dayi" alternating pressure air mattress (unsterilized)
TW: “大億”交替式壓力氣墊床 (未滅菌)
Taiwan·Risk Class 1·Dayi Medical Instrument Factory·Registered May 20, 2009 – May 20, 2014CancelledRegistration details
- Analysis ID
- f627aa773ad3fbb30b43c4de993304fe
Company information
- Manufacturer
- Dayi Medical Instrument Factory
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- Dayi Medical Instrument Factory
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
- Domestic
Dates and status
- Registration Date
- May 20, 2009
- Expiry Date
- May 20, 2014
- Cancellation Date
- Dec 14, 2016
Cancellation information
- Status
- Logged out
- Reason
- 屆期未申請展延
About this record
Access comprehensive regulatory information for "Dayi" 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 f627aa773ad3fbb30b43c4de993304fe and manufactured by Dayi Medical Instrument Factory. The authorized representative in Taiwan is Dayi Medical Instrument Factory.
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