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"General Medicine" Rigid Laryngoscopy (Unsterilized) - Taiwan Registration da6a649f40e607b0771a2e1846e42949

Access comprehensive regulatory information for "General Medicine" Rigid Laryngoscopy (Unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number da6a649f40e607b0771a2e1846e42949 and manufactured by PROACT MEDICAL LTD.. The authorized representative in Taiwan is PHOENIX INSTRUMENT BUSINESS 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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da6a649f40e607b0771a2e1846e42949
Registration Details
Taiwan FDA Registration: da6a649f40e607b0771a2e1846e42949
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Device Details

"General Medicine" Rigid Laryngoscopy (Unsterilized)
TW: "ๆ™ฎ้†ซ" ็กฌๅผๅ–‰้ ญ้ก (ๆœชๆป…่Œ)
Risk Class 1
Cancelled

Registration Details

da6a649f40e607b0771a2e1846e42949

DHA04400933300

Company Information

United Kingdom

Product Details

Limited to the first level of identification scope of the Measures for the Administration of Medical Devices "Rigid Laryngoscopy (D.5540)".

D Anesthesiology

D.5540 Rigid laryngoscope

import

Dates and Status

Oct 08, 2010

Oct 08, 2015

Apr 25, 2018

Cancellation Information

Logged out

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