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"Mizushibi" respirator - Taiwan Registration 976b2c24914311f5d4735774a47d265d

Access comprehensive regulatory information for "Mizushibi" respirator in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 976b2c24914311f5d4735774a47d265d and manufactured by RESMED LIMITED. The authorized representative in Taiwan is BROJAW INC..

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including RESMED LTD., and 1 recent registrations in the same category. 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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976b2c24914311f5d4735774a47d265d
Registration Details
Taiwan FDA Registration: 976b2c24914311f5d4735774a47d265d
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Device Details

"Mizushibi" respirator
TW: "็‘žๅฃซ็พŽ" ๅ‘ผๅธๅ™จ
Risk Class 2
Cancelled

Registration Details

976b2c24914311f5d4735774a47d265d

DHA00601274401

Company Information

Australia

Product Details

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

D Anesthesiology

D.5905 Non-continuous respirators

import

Dates and Status

Oct 20, 2005

Oct 20, 2015

May 17, 2018

Cancellation Information

Logged out

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