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"Termao" Di Di Xun guide set - Taiwan Registration 211428be3733b8f3593ea2dd03496f9b

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 211428be3733b8f3593ea2dd03496f9b and manufactured by TERUMO CORPORATION;; ASHITAKA FACTORY OF TERUMO CORPORATION. The authorized representative in Taiwan is TERUMO TAIWAN MEDICAL 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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211428be3733b8f3593ea2dd03496f9b
Registration Details
Taiwan FDA Registration: 211428be3733b8f3593ea2dd03496f9b
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Device Details

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

Registration Details

211428be3733b8f3593ea2dd03496f9b

DHA05603207805

Company Information

Product Details

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

E Cardiovascular Medicine Science

E.1340 Catheter Introducers

import

Dates and Status

Jan 18, 2019

Jan 18, 2024

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