"STRENGTHEN" Nonpowered flotation therapy mattress (Non-Sterile) - Taiwan Registration ad2a57989617e6302f8a03c9ace1dbaf
Access comprehensive regulatory information for "STRENGTHEN" Nonpowered flotation therapy mattress (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 ad2a57989617e6302f8a03c9ace1dbaf and manufactured by LINET SPOL. S R. O.. The authorized representative in Taiwan is Johnson & Johnson Medical Instruments Inc.
This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including LINET SPOL. S R. O., and 1 recent registrations in the same category. 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.
Device Details
Registration Details
ad2a57989617e6302f8a03c9ace1dbaf
Ministry of Health Medical Device Import Registration No. 021247
DHA08402124702
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, 2025