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"Jimmy" ENT fiber optic light source and vehicle (unsterilized) - Taiwan Registration b8cd9acbda30dfc7565216293edc1faa

Access comprehensive regulatory information for "Jimmy" ENT fiber optic light source and vehicle (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number b8cd9acbda30dfc7565216293edc1faa and manufactured by GIMMI GMBH. The authorized representative in Taiwan is BEAMED INSTRUMENTS 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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b8cd9acbda30dfc7565216293edc1faa
Registration Details
Taiwan FDA Registration: b8cd9acbda30dfc7565216293edc1faa
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Device Details

"Jimmy" ENT fiber optic light source and vehicle (unsterilized)
TW: โ€œๅ‰็ฑณโ€่€ณ้ผปๅ–‰ๅ…‰็บ–ๅ…‰ๆบๅŠ่ผ‰ๅ…ท(ๆœชๆป…่Œ)
Risk Class 1
Cancelled

Registration Details

b8cd9acbda30dfc7565216293edc1faa

DHA04401172305

Company Information

Germany

Product Details

Limited to the first level identification scope of the Measures for the Administration of Medical Devices "ENT Fiber Optic Light Source and Vehicle (G.4350)".

G ENT Science

G.4350 Ear, nose and throat optical fiber light sources and carriers

import

Dates and Status

May 18, 2012

May 18, 2022

Apr 12, 2024

Cancellation Information

Logged out

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