Taiwan FDA registration 45079ad48f9e8b143a756ff47ea7baa6

"Vixelin" otoscopy (unsterilized)

TW: "威栩靈" 耳鏡 (未滅菌)

Taiwan·Risk Class 1·WELCH ALLYN INC.·Registered Mar 20, 2012 – Mar 20, 2027Active

Registration details

Analysis ID: 45079ad48f9e8b143a756ff47ea7baa6
Customs Code: DHA04401150100

Company information

Manufacturer: WELCH ALLYN INC.
Manufacturer Country: United States
Authorized Representative: BIOMEGA INSTRUMENT CO., LTD.

Product details

Intended Use: Limited to the first level identification range of the "Otoscope (G.4770)" of the Administrative Measures for the Classification and Grading of Medical Equipment.
Product Type (Level 1): G ENT Science
Product Type (Level 2): G.4770 Ear Mirrors
Import Information: import

Dates and status

Registration Date: Mar 20, 2012
Expiry Date: Mar 20, 2027

About this record

Access comprehensive regulatory information for "Vixelin" otoscopy (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 45079ad48f9e8b143a756ff47ea7baa6 and manufactured by WELCH ALLYN INC.. The authorized representative in Taiwan is BIOMEGA INSTRUMENT CO., LTD..

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