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"Pentax" intubated fiber optic endoscope - Taiwan Registration de0bb4f8c8366a6918c91d22cb5fbf18

Access comprehensive regulatory information for "Pentax" intubated fiber optic endoscope in Taiwan's medical device market through Pure Global AI's free database. is registered under number de0bb4f8c8366a6918c91d22cb5fbf18 and manufactured by PENTAX TOHOKU CO., 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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de0bb4f8c8366a6918c91d22cb5fbf18
Registration Details
Taiwan FDA Registration: de0bb4f8c8366a6918c91d22cb5fbf18
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Device Details

"Pentax" intubated fiber optic endoscope
TW: "่ณ“ๅพ—ๅฃซ" ๆ’็ฎกๅผๅ…‰็บ–ๅ…ง่ฆ–้ก
Cancelled

Registration Details

de0bb4f8c8366a6918c91d22cb5fbf18

DHA00601426101

Company Information

Japan

Product Details

For details, it is Chinese approved copy of the imitation order

G ENT Science

import

Dates and Status

Apr 10, 2006

Apr 10, 2011

Jul 25, 2014

Cancellation Information

Logged out

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