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"Termao" Di Di Xun guide set - Taiwan Registration a43410a7851609c9d6927061c8584b17

Access comprehensive regulatory information for "Termao" Di Di Xun guide set in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number a43410a7851609c9d6927061c8584b17 and manufactured by TERUMO CORPORATION;; ASHITAKA FACTORY OF TERUMO CORPORATION. The authorized representative in Taiwan is Taipei Branch of Nissho Termo Co., Ltd.

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including TERUMO CORPORATION;; ASHITAKA FACTORY OF TERUMO CORPORATION, and 1 recent registrations in the same category. 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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a43410a7851609c9d6927061c8584b17
Registration Details
Taiwan FDA Registration: a43410a7851609c9d6927061c8584b17
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Device Details

"Termao" Di Di Xun guide set
TW: โ€œๆณฐ็ˆพ่Œ‚โ€่ซฆๆ€่ฟช่ฟ…ๅฐŽๅผ•ๅฅ—
Risk Class 2
Cancelled

Registration Details

a43410a7851609c9d6927061c8584b17

DHA00602125905

Product Details

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

E Cardiovascular Medicine Science

E.1250 Percutaneous catheters

import

Dates and Status

Jul 19, 2010

Jul 19, 2015

Aug 19, 2016

Cancellation Information

Logged out

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