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"Lanyan" Blue crystal porous intervertebral fusion device (lumbar spine) - Taiwan Registration 4431e8c4eabfacad625b4a0cd3b6da42

Access comprehensive regulatory information for "Lanyan" Blue crystal porous intervertebral fusion device (lumbar spine) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 4431e8c4eabfacad625b4a0cd3b6da42 and manufactured by Lanyan Precision Co., Ltd.;; Industrial Technology Research Institute biomedical material products manufacturing plant. The authorized representative in Taiwan is Lanyan Precision Co., Ltd.

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4431e8c4eabfacad625b4a0cd3b6da42
Registration Details
Taiwan FDA Registration: 4431e8c4eabfacad625b4a0cd3b6da42
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Device Details

"Lanyan" Blue crystal porous intervertebral fusion device (lumbar spine)
TW: โ€œ่—็ ”โ€่—ๆ™ถๅคšๅญ”ๅผๆคŽ้–“่žๅˆๅ™จ(่…ฐๆคŽ)
Risk Class 2

Registration Details

4431e8c4eabfacad625b4a0cd3b6da42

Product Details

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

N Orthopedics

N.3080 ๆคŽ้ซ”้–“่žๅˆ่ฃ็ฝฎ

Contract manufacturing;; Domestic

Dates and Status

Feb 01, 2021

Feb 01, 2026