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"TENORTHO" Truncal orthosis (Non-Sterile) - Taiwan Registration bd8c5f9a43fac3cb697c42000f491067

Access comprehensive regulatory information for "TENORTHO" Truncal orthosis (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 bd8c5f9a43fac3cb697c42000f491067 and manufactured by TENORTHO S.R.L. The authorized representative in Taiwan is MENEY CO., LTD..

This page provides complete technical specifications, regulatory compliance details, 2 companies making similar products including TENORTHO S.R.L., TENORTHO S.R.L, and 2 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.

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bd8c5f9a43fac3cb697c42000f491067
Registration Details
Taiwan FDA Registration: bd8c5f9a43fac3cb697c42000f491067
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Device Details

"TENORTHO" Truncal orthosis (Non-Sterile)
TW: "ๅคฉ็ถข" ่ป€ๅนน่ฃๅ…ท (ๆœชๆป…่Œ)
Risk Class 1
MD
Cancelled

Registration Details

bd8c5f9a43fac3cb697c42000f491067

Ministry of Health Medical Device Import No. 018615

DHA09401861504

Company Information

Italy

Product Details

o Equipment for physical medicine

O3490 Torso Gear

Imported from abroad

Dates and Status

Dec 15, 2017

Dec 15, 2022

Cancellation Information

Logged out

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