Taiwan FDA registration 2c41be937e4f80d3c00b935eedb1fa45

"Bin Air" surgical instruments, motors and accessories or accessories (unsterilized)

TW: “賓愛爾”手術用器具馬達與配件或附件 (未滅菌)

Taiwan·Risk Class 1·Bien Air Surgery Ltd·Registered Dec 22, 2011 – Dec 22, 2021Cancelled

Registration details

Analysis ID: 2c41be937e4f80d3c00b935eedb1fa45
Customs Code: DHA04401121104

Company information

Manufacturer: Bien Air Surgery Ltd
Manufacturer Country: Switzerland
Authorized Representative: GOLDENSPRING MEDI-TECH CO., LTD.

Product details

Intended Use: Limited to the first level of identification scope of the Measures for the Administration of Medical Devices "Surgical Instruments, Motors and Accessories or Accessories (I.4820)".
Product Type (Level 1): I General, Plastic Surgery and Dermatology
Product Type (Level 2): I.4820 Surgical Appliances and Accessories or Accessories
Import Information: import

Dates and status

Registration Date: Dec 22, 2011
Expiry Date: Dec 22, 2021
Cancellation Date: Sep 23, 2023

Cancellation information

Status: Logged out
Reason: 自行鍵入

About this record

Access comprehensive regulatory information for "Bin Air" surgical instruments, motors and accessories or accessories (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 2c41be937e4f80d3c00b935eedb1fa45 and manufactured by Bien Air Surgery Ltd. The authorized representative in Taiwan is GOLDENSPRING MEDI-TECH CO., LTD..

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