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"Ambo" otoscopy (unsterilized) - Taiwan Registration fcbccb50593afac0303f8343420d5366

Access comprehensive regulatory information for "Ambo" 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 fcbccb50593afac0303f8343420d5366 and manufactured by RF CO., LTD.. The authorized representative in Taiwan is Zongteng Technology 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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fcbccb50593afac0303f8343420d5366
Registration Details
Taiwan FDA Registration: fcbccb50593afac0303f8343420d5366
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Device Details

"Ambo" otoscopy (unsterilized)
TW: โ€œๅฎ‰ไผโ€่€ณ้ก (ๆœชๆป…่Œ)
Risk Class 1
Cancelled

Registration Details

fcbccb50593afac0303f8343420d5366

DHA04400517909

Company Information

Japan

Product Details

Limited to the first level identification range of the Measures for the Administration of Medical Devices "Otoscope (G.4770)".

G ENT Science

G.4770 Ear Mirrors

import

Dates and Status

Sep 20, 2006

Sep 20, 2011

Nov 27, 2012

Cancellation Information

Logged out

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