Taiwan FDA registration 591cb3df49893fc0924c4f68d1de357e
"ACTION" Nonpowered flotation therapy mattress
TW: "耶訊"非動力式治療床墊
Taiwan·Risk Class 1·MD·ACTION PRODUCTS, INC.·Registered Oct 01, 2021 – Oct 31, 2026ActiveRegistration details
- Analysis ID
- 591cb3df49893fc0924c4f68d1de357e
- License Form
- Ministry of Health Medical Device Import Registration No. 004221
- Customs Code
- DHA08400422100
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)
- J5150 Non-powered treatment mattress
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Oct 01, 2021
- Expiry Date
- Oct 31, 2026
About this record
Access comprehensive regulatory information for "ACTION" Nonpowered flotation therapy mattress in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 591cb3df49893fc0924c4f68d1de357e and manufactured by ACTION PRODUCTS, INC.. The authorized representative in Taiwan is GRAND MEDICAL INSTRUMENT CO., LTD..
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