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"Teleflex" evoked spirometer - Taiwan Registration 31e9d654661aa7066a96e8c05209f4f3

Access comprehensive regulatory information for "Teleflex" evoked spirometer in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 31e9d654661aa7066a96e8c05209f4f3 and manufactured by Teleflex Medical; Teleflex Medical de Mรฉxico, S. de R.L. de C.V.. The authorized representative in Taiwan is K&C MEDICAL 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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31e9d654661aa7066a96e8c05209f4f3
Registration Details
Taiwan FDA Registration: 31e9d654661aa7066a96e8c05209f4f3
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Device Details

"Teleflex" evoked spirometer
TW: โ€œๆณฐๅˆฉ็ฆโ€ ่ช˜็™ผๅž‹่‚บ้‡่จˆ
Risk Class 2

Registration Details

31e9d654661aa7066a96e8c05209f4f3

DHA05603543008

Company Information

Product Details

Details are as detailed as approved Chinese instructions

D Anesthesiology

D.5690 ่ช˜็™ผๅž‹่‚บ้‡่จˆ

import

Dates and Status

May 12, 2022

May 12, 2027