Taiwan FDA registration c5528f947f1cf71159da5828240a6574

"Action" Mattress Overlays (non-sterile)

TW: "艾克森" 減壓床墊 (未滅菌)

Taiwan·Risk Class 1·MD·ACTION PRODUCTS, INC.·Registered Oct 01, 2021 – Oct 31, 2027Active

Registration details

Analysis ID: c5528f947f1cf71159da5828240a6574
License Form: Ministry of Health Medical Device Import Registration No. 011298
Customs Code: DHA08401129800

Company information

Manufacturer: ACTION PRODUCTS, INC.
Manufacturer Country: United States
Authorized Representative: Johnson & Johnson Medical Devices, Inc

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, 2027

About this record

Access comprehensive regulatory information for "Action" Mattress Overlays (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 c5528f947f1cf71159da5828240a6574 and manufactured by ACTION PRODUCTS, INC.. The authorized representative in Taiwan is Johnson & Johnson Medical Devices, Inc.

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.