Taiwan FDA registration d84121b1d432f7a4c97ecc1b77203e8b

"Euro Fisther" spinal endoscopy tool (unsterilized)

TW: "歐御費絲特" 脊椎內視鏡工具 (未滅菌)

Taiwan·Risk Class 1·BAUI BIOTECH CO., LTD.·Registered Jul 04, 2016 – Jul 04, 2021Cancelled

Registration details

Analysis ID: d84121b1d432f7a4c97ecc1b77203e8b

Company information

Manufacturer: BAUI BIOTECH CO., LTD.
Manufacturer Country: Taiwan, Province of China
Authorized Representative: EUROPE ROYAL MEDICAL DEVICES INDUSTRIAL 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 Orthopedics
Product Type (Level 2): N.1100 Closing Lenses
Import Information: Domestic;; Contract manufacturing

Dates and status

Registration Date: Jul 04, 2016
Expiry Date: Jul 04, 2021
Cancellation Date: Jun 22, 2022

Cancellation information

Status: Logged out
Reason: 許可證已逾有效期

About this record

Access comprehensive regulatory information for "Euro Fisther" spinal endoscopy tool (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number d84121b1d432f7a4c97ecc1b77203e8b and manufactured by BAUI BIOTECH CO., LTD.. The authorized representative in Taiwan is EUROPE ROYAL MEDICAL DEVICES INDUSTRIAL CO., LTD..

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