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Breelib Inhalation System - Taiwan Registration 8448cc2f306a3f18b9d79878a0da7a31

Access comprehensive regulatory information for Breelib Inhalation System in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 8448cc2f306a3f18b9d79878a0da7a31 and manufactured by Vectura Group Ltd. The authorized representative in Taiwan is BAYER TAIWAN COMPANY 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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8448cc2f306a3f18b9d79878a0da7a31
Registration Details
Taiwan FDA Registration: 8448cc2f306a3f18b9d79878a0da7a31
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Device Details

Breelib Inhalation System
TW: ๅ‚™ๅˆฉๅธๅ…ฅ็ณป็ตฑ
Risk Class 2
MD

Registration Details

8448cc2f306a3f18b9d79878a0da7a31

Ministry of Health Medical Device Import No. 031202

DHA05603120201

Company Information

United Kingdom

Product Details

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

D Devices for anesthesiology

D5630 Sprayer

Imported from abroad

Dates and Status

Jun 26, 2018

Jun 26, 2028