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"Flex" non-contact respiratory rate monitoring system - Taiwan Registration c7f890df48bfa0909edf2ef9c428851b

Access comprehensive regulatory information for "Flex" non-contact respiratory rate 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 c7f890df48bfa0909edf2ef9c428851b and manufactured by WISTRON MEDICAL TECHNOLOGY CORPORATION. The authorized representative in Taiwan is WISTRON MEDICAL TECHNOLOGY CORPORATION.

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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c7f890df48bfa0909edf2ef9c428851b
Registration Details
Taiwan FDA Registration: c7f890df48bfa0909edf2ef9c428851b
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Device Details

"Flex" non-contact respiratory rate monitoring system
TW: "้†ซๅ€ๆ€"้žๆŽฅ่งธๅผๅ‘ผๅธ้ ป็އ็›ฃๆธฌ็ณป็ตฑ
Risk Class 2

Registration Details

c7f890df48bfa0909edf2ef9c428851b

Company Information

Taiwan, Province of China

Product Details

Details are as detailed as approved Chinese instructions

D Anesthesiology; E Cardiovascular Medicine Science

E.2910 Receivers for Physiological Signal Transmission by Radio Waves;; D.2375 Respiratory Rate Monitor

Domestic

Dates and Status

Jul 23, 2023

Jul 23, 2028