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"Dry" bone plate system - Taiwan Registration 2fa43e1975a4b43fc7b9ceff0e0a4e3e

Access comprehensive regulatory information for "Dry" bone plate system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 2fa43e1975a4b43fc7b9ceff0e0a4e3e and manufactured by Dry Biomedical Technology Co., Ltd. Forest Factory. The authorized representative in Taiwan is Dry Biomedical Technology 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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2fa43e1975a4b43fc7b9ceff0e0a4e3e
Registration Details
Taiwan FDA Registration: 2fa43e1975a4b43fc7b9ceff0e0a4e3e
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Device Details

"Dry" bone plate system
TW: โ€œไนพ็”Ÿโ€้ชจๆฟ็ณป็ตฑ
Risk Class 2
Cancelled

Registration Details

2fa43e1975a4b43fc7b9ceff0e0a4e3e

DHY00500285306

Company Information

Taiwan, Province of China

Product Details

For details, it is Chinese approved copy of the imitation order

N Orthopedics

N.3030 Single or multiple metallic bone fixation devices and accessories

Domestic

Dates and Status

Dec 15, 2009

Dec 15, 2014

Apr 25, 2018

Cancellation Information

Logged out

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