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Cardiopulmonary function test recorder - Taiwan Registration 6f7e2dcccf9e5655cdaa31bba5af0ab0

Access comprehensive regulatory information for Cardiopulmonary function test recorder in Taiwan's medical device market through Pure Global AI's free database. is registered under number 6f7e2dcccf9e5655cdaa31bba5af0ab0 and manufactured by QUINTON INSTRUMENT CO.. The authorized representative in Taiwan is Pomei Enterprise 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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6f7e2dcccf9e5655cdaa31bba5af0ab0
Registration Details
Taiwan FDA Registration: 6f7e2dcccf9e5655cdaa31bba5af0ab0
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Device Details

Cardiopulmonary function test recorder
TW: ๅฟƒ่‚บๅŠŸ่ƒฝๆธฌ่ฉฆ่จ˜้Œ„ๅ™จ
Cancelled

Registration Details

6f7e2dcccf9e5655cdaa31bba5af0ab0

DHA00600578001

Company Information

United States

Product Details

0211 Pulmonary function tester

import

Dates and Status

Dec 29, 1989

Dec 29, 1994

Oct 06, 1999

Cancellation Information

Logged out

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