Taiwan FDA registration 4431e8c4eabfacad625b4a0cd3b6da42

"Lanyan" Blue crystal porous intervertebral fusion device (lumbar spine)

TW: “藍研”藍晶多孔式椎間融合器(腰椎)
Taiwan flagTaiwan·Risk Class 2·Lanyan Precision Co., Ltd.;; Industrial Technology Research Institute biomedical material products manufacturing plant·Registered Feb 01, 2021 – Feb 01, 2026Expired
Registration details
Analysis ID
4431e8c4eabfacad625b4a0cd3b6da42
Company information
Manufacturer Country
Taiwan, Province of China
Authorized Representative
Lanyan Precision Co., Ltd
Product details
Intended Use
For details, it is Chinese approved copy of the imitation order
Product Type (Level 1)
N Orthopedics
Product Type (Level 2)
N.3080 椎體間融合裝置
Import Information
Contract manufacturing;; Domestic
Dates and status
Registration Date
Feb 01, 2021
Expiry Date
Feb 01, 2026
About this record

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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