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"Gisper" otoscopy (unsterilized) - Taiwan Registration e8be7fc2a79113592e7c22bf53289309

Access comprehensive regulatory information for "Gisper" 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 e8be7fc2a79113592e7c22bf53289309 and manufactured by GIMMI GMBH.. The authorized representative in Taiwan is GRAND MEDICAL 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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e8be7fc2a79113592e7c22bf53289309
Registration Details
Taiwan FDA Registration: e8be7fc2a79113592e7c22bf53289309
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Device Details

"Gisper" otoscopy (unsterilized)
TW: โ€œๅ‰้Šคโ€่€ณ้ก(ๆœชๆป…่Œ๏ผ‰
Risk Class 1

Registration Details

e8be7fc2a79113592e7c22bf53289309

DHA04400913002

Company Information

Germany

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

Aug 25, 2010

Aug 25, 2025