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Mah Respirator - Taiwan Registration fdd1bc096bac4b093fadce0922fd28dc

Access comprehensive regulatory information for Mah Respirator in Taiwan's medical device market through Pure Global AI's free database. is registered under number fdd1bc096bac4b093fadce0922fd28dc and manufactured by PENLON LTD.. The authorized representative in Taiwan is Sankyo Trading Co., Ltd.

This page provides complete technical specifications, regulatory compliance details, 5 companies making similar products including KIMURA MEDICAL INSTRUMENT CO. LTD., MEGAMED AG ELECTRO-MEDINIZISCHE APPARATE, and 5 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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fdd1bc096bac4b093fadce0922fd28dc
Registration Details
Taiwan FDA Registration: fdd1bc096bac4b093fadce0922fd28dc
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Device Details

Mah Respirator
TW: ้บป้†‰ๅ‘ผๅธๅ™จ
Cancelled

Registration Details

fdd1bc096bac4b093fadce0922fd28dc

DHA00600453101

Company Information

United Kingdom

Product Details

0101 Anesthesia apparatus

import

Dates and Status

Jan 21, 1987

Jan 21, 1992

Oct 07, 1999

Cancellation Information

Logged out

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