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"ACTION" Nonpowered flotation therapy mattress - Taiwan Registration 591cb3df49893fc0924c4f68d1de357e

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..

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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591cb3df49893fc0924c4f68d1de357e
Registration Details
Taiwan FDA Registration: 591cb3df49893fc0924c4f68d1de357e
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Device Details

"ACTION" Nonpowered flotation therapy mattress
TW: "่€ถ่จŠ"้žๅ‹•ๅŠ›ๅผๆฒป็™‚ๅบŠๅขŠ
Risk Class 1
MD

Registration Details

591cb3df49893fc0924c4f68d1de357e

Ministry of Health Medical Device Import Registration No. 004221

DHA08400422100

Company Information

United States

Product Details

Limited to the first level identification scope of the Measures for the Administration of Medical Devices "Non-powered Therapeutic Mattresses (J.5150)".

J General hospital and personal use equipment

J5150 Non-powered treatment mattress

Imported from abroad

Dates and Status

Oct 01, 2021

Oct 31, 2026