Taiwan FDA registration b92281731b51cfd6c29e7940c42a284c

Sirius Lumbar Intervertebral Cage

TW: 喜瑞斯腰椎椎間融合器

Taiwan·Risk Class 2·MD·BAUI BIOTECH CO., LTD.·Registered Aug 30, 2021 – Feb 05, 2026Expired

Registration details

Analysis ID: b92281731b51cfd6c29e7940c42a284c
License Form: Ministry of Health Medical Device Manufacturing No. 007180

Company information

Manufacturer: BAUI BIOTECH CO., LTD.
Manufacturer Country: Taiwan, Province of China
Authorized Representative: BAUI BIOTECH CO., LTD.

Product details

Intended Use: Details are as detailed as approved Chinese instructions
Product Type (Level 1): N Orthopedic devices
Product Type (Level 2): N3080 Interbody fusion device
Import Information: Produced in Taiwan, China

Dates and status

Registration Date: Aug 30, 2021
Expiry Date: Feb 05, 2026

About this record

Access comprehensive regulatory information for Sirius Lumbar Intervertebral Cage in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number b92281731b51cfd6c29e7940c42a284c and manufactured by BAUI BIOTECH CO., LTD.. The authorized representative in Taiwan is BAUI BIOTECH CO., LTD..

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