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"Rudolph" otoscopy (unsterilized) - Taiwan Registration bcb4a970e3b1c485f0c5c1b99d8d88ff

Access comprehensive regulatory information for "Rudolph" 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 bcb4a970e3b1c485f0c5c1b99d8d88ff and manufactured by RUDOLF MEDICAL GMBH + CO. KG. The authorized representative in Taiwan is EVERMED INTERNATIONAL 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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bcb4a970e3b1c485f0c5c1b99d8d88ff
Registration Details
Taiwan FDA Registration: bcb4a970e3b1c485f0c5c1b99d8d88ff
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Device Details

"Rudolph" otoscopy (unsterilized)
TW: ใ€้ญฏ้“ๅคซใ€ž ่€ณ้ก (ๆœชๆป…่Œ)
Risk Class 1
Cancelled

Registration Details

bcb4a970e3b1c485f0c5c1b99d8d88ff

DHA04401201904

Company Information

Germany

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

Aug 03, 2012

Aug 03, 2022

Apr 12, 2024

Cancellation Information

Logged out

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