Taiwan FDA registration adb1bc02294a13ec9f3e5bc16f2d2cac

"BAUI" Spinal Endoscopic Instruments (Non-sterile)

TW: "寶億" 脊椎內視鏡工具 (未滅菌)

Taiwan·Risk Class 1·MD·BAUI BIOTECH CO., LTD.·Registered Aug 19, 2019 – Aug 19, 2024Expired

Registration details

Analysis ID: adb1bc02294a13ec9f3e5bc16f2d2cac
License Form: Ministry of Health Medical Device Manufacturing No. 007903

Company information

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

Product details

Intended Use: Limited to the first level identification range of "Arthroscopy (N.1100)" of the Measures for the Administration of Medical Equipment.
Product Type (Level 1): N Orthopedic devices
Product Type (Level 2): N1100 Arthroscopy
Import Information: Produced in Taiwan, China

Dates and status

Registration Date: Aug 19, 2019
Expiry Date: Aug 19, 2024

About this record

Access comprehensive regulatory information for "BAUI" Spinal Endoscopic Instruments (Non-sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number adb1bc02294a13ec9f3e5bc16f2d2cac and manufactured by BAUI BIOTECH CO., LTD.. The authorized representative in Taiwan is BAUI BIOTECH CO., LTD..

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