Taiwan FDA registration 94845c180db20eda1f5ee82997df07db

"BAUI" Orthopedic manual surgical instrument (Non-Sterile)

TW: "寶億" 手動式骨科手術器械 (未滅菌)

Taiwan·Risk Class 1·MD·BAUI BIOTECH CO., LTD.·Registered Mar 15, 2018 – Mar 15, 2028Active

Registration details

Analysis ID: 94845c180db20eda1f5ee82997df07db
License Form: Ministry of Health Medical Device Manufacturing No. 007169

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 manual orthopedic surgical instruments (N.4540) of the Measures for the Administration of Medical Equipment.
Product Type (Level 1): N Orthopedic devices
Product Type (Level 2): N4540 Manual osteologic surgery instrument
Import Information: Produced in Taiwan, China

Dates and status

Registration Date: Mar 15, 2018
Expiry Date: Mar 15, 2028

About this record

Access comprehensive regulatory information for "BAUI" Orthopedic manual surgical instrument (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 94845c180db20eda1f5ee82997df07db and manufactured by BAUI BIOTECH CO., LTD.. The authorized representative in Taiwan is BAUI BIOTECH CO., LTD..

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