Taiwan FDA registration ac6bf83e25d56bde04fa6679efd96c60

"Leading" polymer intervertebral fusion device for endoscopy

TW: “先銳” 內視鏡用高分子椎間融合器

Taiwan·Risk Class 2·CHANPIN MEDTAK CO., LTD.·Registered Oct 07, 2022 – Oct 07, 2027Active

Registration details

Analysis ID: ac6bf83e25d56bde04fa6679efd96c60

Company information

Manufacturer: CHANPIN MEDTAK CO., LTD.
Manufacturer Country: Taiwan, Province of China
Authorized Representative: BAT TECHNOLOGY CO., LTD.

Product details

Intended Use: Details are as detailed as approved Chinese instructions
Product Type (Level 1): N Orthopedics
Product Type (Level 2): N.3080 椎體間融合裝置
Import Information: Domestic;; Contract manufacturing

Dates and status

Registration Date: Oct 07, 2022
Expiry Date: Oct 07, 2027

About this record

Access comprehensive regulatory information for "Leading" polymer intervertebral fusion device for endoscopy in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number ac6bf83e25d56bde04fa6679efd96c60 and manufactured by CHANPIN MEDTAK CO., LTD.. The authorized representative in Taiwan is BAT TECHNOLOGY CO., LTD..

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