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"Asahi" Restrix hollow dialyzer - Taiwan Registration e54acb13d87a5e9d54ddc38ecbf1fd76

Access comprehensive regulatory information for "Asahi" Restrix hollow dialyzer in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number e54acb13d87a5e9d54ddc38ecbf1fd76 and manufactured by Asahi Kasei Medical Co., Ltd. Okatomi Plant. The authorized representative in Taiwan is Taiwan Asahi Kasei Medical Device Trading 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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e54acb13d87a5e9d54ddc38ecbf1fd76
Registration Details
Taiwan FDA Registration: e54acb13d87a5e9d54ddc38ecbf1fd76
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Device Details

"Asahi" Restrix hollow dialyzer
TW: โ€œๆ—ญโ€็‘žๆ–ฏ็‰นๅˆฉๅ…‹ๆ–ฏไธญ็ฉบ็ณปๅž‹้€ๆžๅ™จ
Risk Class 2
Cancelled

Registration Details

e54acb13d87a5e9d54ddc38ecbf1fd76

DHA00602336909

Product Details

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

H Gastroenterology and urology

H.5820 ่ก€ๆถฒ้€ๆž็ณป็ตฑๅŠๅ…ถ้™„ไปถ

import

Dates and Status

Mar 08, 2012

Mar 08, 2017

Jan 28, 2016

Cancellation Information

Logged out

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