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"Bionet" Diagnostic spirometer - Taiwan Registration d130dc6da4e619899508e04d2888bb37

Access comprehensive regulatory information for "Bionet" Diagnostic spirometer in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number d130dc6da4e619899508e04d2888bb37 and manufactured by Bionet Co., Ltd.. The authorized representative in Taiwan is MEDWAY BME 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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d130dc6da4e619899508e04d2888bb37
Registration Details
Taiwan FDA Registration: d130dc6da4e619899508e04d2888bb37
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Device Details

"Bionet" Diagnostic spirometer
TW: "็™พ่ƒฝ็‰น" ่จบๆ–ท็”จ่‚บ้‡่จˆ
Risk Class 2
MD

Registration Details

d130dc6da4e619899508e04d2888bb37

Ministry of Health Medical Device Import No. 035136

DHA05603513608

Company Information

Korea, Republic of

Product Details

Details are as detailed as approved Chinese instructions

D Anesthesiology

D1840 Spirometer for diagnosis

Imported from abroad

Dates and Status

Jan 20, 2022

Jan 20, 2027