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Knooda right heart diagnostic catheter - Taiwan Registration db7b6a3a5760b491279a661839414037

Access comprehensive regulatory information for Knooda right heart diagnostic catheter in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number db7b6a3a5760b491279a661839414037 and manufactured by AESCULAP CHIFA SP. Z O.O.;; B. BRAUN MELSUNGEN AG. The authorized representative in Taiwan is B. BRAUN 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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db7b6a3a5760b491279a661839414037
Registration Details
Taiwan FDA Registration: db7b6a3a5760b491279a661839414037
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Device Details

Knooda right heart diagnostic catheter
TW: ๅ…‹่ซพ้”ๅณๅฟƒ่จบๆ–ทๅฐŽ็ฎก
Risk Class 2
Cancelled

Registration Details

db7b6a3a5760b491279a661839414037

DHA00602332301

Company Information

Product Details

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

E Cardiovascular Medicine Science

E.1200 ่จบๆ–ท็”จ่ก€็ฎกๅ…งๅฐŽ็ฎก

import

Dates and Status

Apr 24, 2012

Apr 24, 2017

Nov 20, 2019

Cancellation Information

Logged out

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