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"EMANA" Limb orthosis (Non-Sterile) - Taiwan Registration 2161b4113e32133b493585d3d74c287c

Access comprehensive regulatory information for "EMANA" Limb 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 2161b4113e32133b493585d3d74c287c and manufactured by SHENGDEI TECHNOLOGY CO., LTD.. The authorized representative in Taiwan is Riteng Biomedical 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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2161b4113e32133b493585d3d74c287c
Registration Details
Taiwan FDA Registration: 2161b4113e32133b493585d3d74c287c
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Device Details

"EMANA" Limb orthosis (Non-Sterile)
TW: "ๆ—ฅๆป•" ่‚ข้ซ”่ฃๅ…ท (ๆœชๆป…่Œ)
Risk Class 1
MD
Cancelled

Registration Details

2161b4113e32133b493585d3d74c287c

Ministry of Health Medical Device Manufacturing No. 007959

Company Information

Taiwan, Province of China

Product Details

o Equipment for physical medicine

O3475 Body Equipment

Produced in Taiwan, China; Contract manufacturing

Dates and Status

Sep 19, 2019

Sep 19, 2024

Cancellation Information

Logged out

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