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"Swiss Bo" reinhalation device (unsterilized) - Taiwan Registration 11d225d10f2870e468f4539e47889e65

Access comprehensive regulatory information for "Swiss Bo" reinhalation device (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 11d225d10f2870e468f4539e47889e65 and manufactured by RESPIRONICS, INC.. The authorized representative in Taiwan is BROJAW INC..

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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11d225d10f2870e468f4539e47889e65
Registration Details
Taiwan FDA Registration: 11d225d10f2870e468f4539e47889e65
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Device Details

"Swiss Bo" reinhalation device (unsterilized)
TW: "็‘žๅฃซๅš" ๅ†ๅธๅ…ฅ่ฃ็ฝฎ(ๆœชๆป…่Œ)
Risk Class 1
Cancelled

Registration Details

11d225d10f2870e468f4539e47889e65

DHA04400421600

Company Information

United States

Product Details

D Anesthesiology

D.5675 Re-inhalation device

import

Dates and Status

Apr 25, 2006

Apr 25, 2016

May 17, 2018

Cancellation Information

Logged out

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