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"Baonan" Lockma interridge decompression system - Taiwan Registration f60020d7cc34a5f8e49e1c0a5b501689

Access comprehensive regulatory information for "Baonan" Lockma interridge decompression system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number f60020d7cc34a5f8e49e1c0a5b501689 and manufactured by PAONAN BIOTECH CO., LTD.. The authorized representative in Taiwan is PAONAN BIOTECH CO., LTD..

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f60020d7cc34a5f8e49e1c0a5b501689
Registration Details
Taiwan FDA Registration: f60020d7cc34a5f8e49e1c0a5b501689
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Device Details

"Baonan" Lockma interridge decompression system
TW: โ€œๅฏถๆฅ โ€ๆด›ๅ…‹้ฆฌ่„Š็ช้–“ๆธ›ๅฃ“็ณป็ตฑ
Risk Class 2

Registration Details

f60020d7cc34a5f8e49e1c0a5b501689

Company Information

Taiwan, Province of China

Product Details

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

N Orthopedics

N.3050 ๆคŽๅผ“ๆฟ้–“ไน‹่„ŠๆคŽ็Ÿฏๆญฃๅ›บๅฎš็‰ฉ

Domestic

Dates and Status

Apr 10, 2013

Apr 10, 2028