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"Apatek" Pentax Light Source and Accessories (Unsterilized) - Taiwan Registration 566929797c9c3d1ddcb93f29defa2745

Access comprehensive regulatory information for "Apatek" Pentax Light Source and Accessories (Unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 566929797c9c3d1ddcb93f29defa2745 and manufactured by APPLITEC LTD.. The authorized representative in Taiwan is WHOLE WELL 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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566929797c9c3d1ddcb93f29defa2745
Registration Details
Taiwan FDA Registration: 566929797c9c3d1ddcb93f29defa2745
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Device Details

"Apatek" Pentax Light Source and Accessories (Unsterilized)
TW: โ€œ้˜ฟๅธ•ๆณฐๅ…‹โ€่ณ“ๅพ—ๅฃซๅ…‰ๆบๅŠ้™„ไปถ (ๆœชๆป…่Œ)
Risk Class 1
Cancelled

Registration Details

566929797c9c3d1ddcb93f29defa2745

DHA04400511203

Company Information

Israel

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

Sep 01, 2006

Sep 01, 2011

Jul 25, 2014

Cancellation Information

Logged out

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