Taiwan FDA registration 2fd5caafd60721336a198f947789af1f

Macrocervical intervertebral fusion device

TW: 群力頸椎椎間融合器

Taiwan·Risk Class 2·Guanya Biotechnology Co., Ltd. new store factory·Registered Mar 06, 2013 – Mar 06, 2028Active

Registration details

Analysis ID: 2fd5caafd60721336a198f947789af1f

Company information

Manufacturer: Guanya Biotechnology Co., Ltd. new store factory
Manufacturer Country: Taiwan, Province of China
Authorized Representative: GROUP INNOMED BIOTECH 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.3060 椎體間之脊椎矯正固定物
Import Information: Contract manufacturing;; Domestic

Dates and status

Registration Date: Mar 06, 2013
Expiry Date: Mar 06, 2028

About this record

Access comprehensive regulatory information for Macrocervical intervertebral fusion device in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 2fd5caafd60721336a198f947789af1f and manufactured by Guanya Biotechnology Co., Ltd. new store factory. The authorized representative in Taiwan is GROUP INNOMED BIOTECH CO., LTD..

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