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"Vixelin" otoscopy (unsterilized) - Taiwan Registration 45079ad48f9e8b143a756ff47ea7baa6

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..

This page provides complete technical specifications, regulatory compliance details. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.

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45079ad48f9e8b143a756ff47ea7baa6
Registration Details
Taiwan FDA Registration: 45079ad48f9e8b143a756ff47ea7baa6
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Device Details

"Vixelin" otoscopy (unsterilized)
TW: "ๅจๆ ฉ้ˆ" ่€ณ้ก (ๆœชๆป…่Œ)
Risk Class 1

Registration Details

45079ad48f9e8b143a756ff47ea7baa6

DHA04401150100

Company Information

United States

Product Details

Limited to the first level identification range of the "Otoscope (G.4770)" of the Administrative Measures for the Classification and Grading of Medical Equipment.

G ENT Science

G.4770 Ear Mirrors

import

Dates and Status

Mar 20, 2012

Mar 20, 2027