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"Mesi-drymother" platelet storage system - Taiwan Registration 7e1eb908f52fdcef53bb2a75aa0f1278

Access comprehensive regulatory information for "Mesi-drymother" platelet storage system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 7e1eb908f52fdcef53bb2a75aa0f1278 and manufactured by MEDIKAN CO. LTD.. The authorized representative in Taiwan is Robbie Jenny International Inc.

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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7e1eb908f52fdcef53bb2a75aa0f1278
Registration Details
Taiwan FDA Registration: 7e1eb908f52fdcef53bb2a75aa0f1278
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Device Details

"Mesi-drymother" platelet storage system
TW: โ€œ็พŽๆ–ฏๅนนๆฏโ€่ก€ๅฐๆฟ่ฒฏๅญ˜็ณป็ตฑ
Risk Class 1
Cancelled

Registration Details

7e1eb908f52fdcef53bb2a75aa0f1278

DHA04400849508

Company Information

Korea, Republic of

Product Details

Limited to the first level identification scope of the Measures for the Administration of Medical Devices "Containers for Preserving Platelet Concentrate (B.9575)".

B Hematology, pathology, and genetics

B.9575 Environmental control chamber for storing platelet concentrate

import

Dates and Status

Jan 28, 2010

Jan 28, 2015

Jul 09, 2015

Cancellation Information

Logged out

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