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"Meibo" infusion sleeve - Taiwan Registration a502741730237371d29986237cabf305

Access comprehensive regulatory information for "Meibo" infusion sleeve in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number a502741730237371d29986237cabf305 and manufactured by MEDPRO INTERNATIONAL (THAILAND) LTD.. The authorized representative in Taiwan is FISOMED TAIWAN 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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a502741730237371d29986237cabf305
Registration Details
Taiwan FDA Registration: a502741730237371d29986237cabf305
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Device Details

"Meibo" infusion sleeve
TW: โ€œ็พŽๅšโ€่ผธๆถฒๅฅ—
Risk Class 2
Cancelled

Registration Details

a502741730237371d29986237cabf305

DHA00601815802

Company Information

Product Details

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

J General hospital and personal use equipment

J.5430 ้ž้›ปๅ‹•ๅผๆถฒ้ซ”ๆณจๅฐ„ๅ™จ

import

Dates and Status

Jul 10, 2007

Jul 10, 2012

Jul 25, 2014

Cancellation Information

Logged out

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