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"Zentek" digital monitoring system - Taiwan Registration 813ff323b74cd1943f005b0828108810

Access comprehensive regulatory information for "Zentek" digital monitoring system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 813ff323b74cd1943f005b0828108810 and manufactured by SENTEC AG. The authorized representative in Taiwan is BROJAW INC..

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including SENTEC AG, 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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813ff323b74cd1943f005b0828108810
Registration Details
Taiwan FDA Registration: 813ff323b74cd1943f005b0828108810
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Device Details

"Zentek" digital monitoring system
TW: โ€œๆ“…็‰นๅ…‹โ€ๆ•ธไฝ็›ฃๆธฌ็ณป็ตฑ
Risk Class 2

Registration Details

813ff323b74cd1943f005b0828108810

DHA05602620500

Company Information

Switzerland

Product Details

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

D Anesthesiology; E Cardiovascular Medicine Science

E.2710 ่€ณๅผ่ก€ๆฐง้ฃฝๅ’Œๆธฌๅฎšๅ„€;; D.2480 ็šฎ่†š่กจ้ขไบŒๆฐงๅŒ–็ขณ็›ฃ่ฆ–ๅ™จ(้žไพตๅ…ฅๅผ);; E.2700 ่ก€ๆฐง้ฃฝๅ’Œๆธฌๅฎšๅ„€

import

Dates and Status

May 20, 2014

May 20, 2029

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