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"Teknor" light sources and vehicles (unsterilized) - Taiwan Registration 042277adf682adb53f7e5d135089d8a5

Access comprehensive regulatory information for "Teknor" light sources and vehicles (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 042277adf682adb53f7e5d135089d8a5 and manufactured by TEKNO-MEDICAL OPTIK-CHIRURGIE GMBH.. The authorized representative in Taiwan is BIOLAND ENTERPRISE INC..

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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042277adf682adb53f7e5d135089d8a5
Registration Details
Taiwan FDA Registration: 042277adf682adb53f7e5d135089d8a5
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Device Details

"Teknor" light sources and vehicles (unsterilized)
TW: "้ตๅ…‹่ซพ" ๅ…‰ๆบๅŠ่ผ‰ๅ…ท (ๆœชๆป…่Œ)
Risk Class 1
Cancelled

Registration Details

042277adf682adb53f7e5d135089d8a5

DHA04401092400

Company Information

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

Oct 11, 2011

Oct 11, 2021

Oct 12, 2023

Cancellation Information

Logged out

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