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Hollow fibrous plasma separator - Taiwan Registration 66c47afefc6a9972318973ab3a71ce69

Access comprehensive regulatory information for Hollow fibrous plasma separator in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 66c47afefc6a9972318973ab3a71ce69 and manufactured by GAMBRO DIALYZER GMBH. The authorized representative in Taiwan is BAXTER HEALTHCARE 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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66c47afefc6a9972318973ab3a71ce69
Registration Details
Taiwan FDA Registration: 66c47afefc6a9972318973ab3a71ce69
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Device Details

Hollow fibrous plasma separator
TW: ไธญ็ฉบ็บ–็ถญๅž‹่ก€ๆผฟๅˆ†้›ขๅ™จ
Risk Class 2

Registration Details

66c47afefc6a9972318973ab3a71ce69

DHA00600603002

Company Information

Germany

Product Details

0399 Other artificial function substitutes

import

Dates and Status

Aug 14, 1990

Feb 09, 2024