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"Teknor" light source and vehicle (unsterilized) - Taiwan Registration ec5edc8b51d51cb620ff05fe4fe637f1

Access comprehensive regulatory information for "Teknor" 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 ec5edc8b51d51cb620ff05fe4fe637f1 and manufactured by TEKNO-MEDICAL OPTIK-CHIRURGIE GMBH & CO. KG. 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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ec5edc8b51d51cb620ff05fe4fe637f1
Registration Details
Taiwan FDA Registration: ec5edc8b51d51cb620ff05fe4fe637f1
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Device Details

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

Registration Details

ec5edc8b51d51cb620ff05fe4fe637f1

DHA04400430002

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

May 01, 2006

May 01, 2011

Nov 04, 2011

Cancellation Information

Logged out

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