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"Baide" Fenwal plasma pressure plate (unsterilized) - Taiwan Registration 24b68d5f4249801ee6cd46a8880a710f

Access comprehensive regulatory information for "Baide" Fenwal plasma pressure plate (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 24b68d5f4249801ee6cd46a8880a710f and manufactured by BAXTER HEALTHCARE CORPORATION. The authorized representative in Taiwan is Y.H. BIOTEK 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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24b68d5f4249801ee6cd46a8880a710f
Registration Details
Taiwan FDA Registration: 24b68d5f4249801ee6cd46a8880a710f
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Device Details

"Baide" Fenwal plasma pressure plate (unsterilized)
TW: โ€œไฝฐๅพทโ€่Šฌๆฒƒ่ก€ๆผฟๅฃ“ๆฟ (ๆœชๆป…่Œ)
Risk Class 1
Cancelled

Registration Details

24b68d5f4249801ee6cd46a8880a710f

DHA04400797300

Company Information

United States

Product Details

The blood component pressure device can separate various blood components from the whole blood after centrifugation, and does not contain sensors and weighing devices.

B Hematology, pathology, and genetics

B.9050 Blood bank supply equipment

import

Dates and Status

Aug 20, 2009

Aug 20, 2014

Jun 28, 2018

Cancellation Information

Logged out

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