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“Hausmann” Plinth (Non-Sterile) - Taiwan Registration c6f568ea805655eaf2ed45ce302c135b

Access comprehensive regulatory information for “Hausmann” Plinth (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 c6f568ea805655eaf2ed45ce302c135b and manufactured by HAUSMANN INDUSTREIS, INC.. The authorized representative in Taiwan is GOOD LINE INCORPORATION.

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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c6f568ea805655eaf2ed45ce302c135b
Registration Details
Taiwan FDA Registration: c6f568ea805655eaf2ed45ce302c135b
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Device Details

“Hausmann” Plinth (Non-Sterile)
TW: “哈士門” 治療檯 (未滅菌)
Risk Class 1
MD

Registration Details

c6f568ea805655eaf2ed45ce302c135b

Ministry of Health Medical Device Import Registration No. a00022

DHA084a0002207

Company Information

United States

Product Details

o Physical Medical Sciences

O3520 treatment unit

Dates and Status

Nov 11, 2021

Oct 31, 2023

Dec 07, 2022