Taiwan FDA registration a1bc9641e71ee841fd5fd035567b80b1
"Yesun" non-powered treatment mattress
TW: "耶訊"非動力式治療床墊
Registration details
- Analysis ID
- a1bc9641e71ee841fd5fd035567b80b1
- Customs Code
- DHA04400422103
Company information
- Manufacturer
- ACTION PRODUCTS, INC.
- Manufacturer Country
- United States
- Authorized Representative
- GRAND MEDICAL INSTRUMENT CO., LTD.
Product details
- Intended Use
- Limited to the first level identification scope of the Measures for the Administration of Medical Devices "Non-powered Therapeutic Mattresses (J.5150)".
- Product Type (Level 1)
- J General hospital and personal use equipment
- Product Type (Level 2)
- J.5150 Non-powered floating therapy mattress
- Import Information
- import
Dates and status
- Registration Date
- Apr 26, 2006
- Expiry Date
- Apr 26, 2026
- Cancellation Date
- Sep 30, 2021
Cancellation information
- Status
- Logged out
- Reason
- 轉為登錄字號
About this record
Access comprehensive regulatory information for "Yesun" non-powered treatment mattress in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number a1bc9641e71ee841fd5fd035567b80b1 and manufactured by ACTION PRODUCTS, INC.. The authorized representative in Taiwan is GRAND MEDICAL INSTRUMENT CO., 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.
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