Taiwan FDA registration 1da9bd8472864d3907d9c20dc6301c38

"VIES" surgical instruments, motors with accessories or accessories (unsterilized)

TW: “威力斯”手術用器具馬達與配件或附件 (未滅菌)

Taiwan·Risk Class 1·VILEX, INC.·Registered May 29, 2006 – May 29, 2016Cancelled

Registration details

Analysis ID: 1da9bd8472864d3907d9c20dc6301c38
Customs Code: DHA04400461906

Company information

Manufacturer: VILEX, INC.
Manufacturer Country: United States
Authorized Representative: Conservation Corporation Limited

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: May 29, 2006
Expiry Date: May 29, 2016
Cancellation Date: Jun 25, 2018

Cancellation information

Status: Logged out
Reason: 許可證已逾有效期

About this record

Access comprehensive regulatory information for "VIES" surgical instruments, motors with 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 1da9bd8472864d3907d9c20dc6301c38 and manufactured by VILEX, INC.. The authorized representative in Taiwan is Conservation Corporation Limited.

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