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"Biumoni" respirator - Taiwan Registration f5010d8d27f480ff58d70349eedc9035

Access comprehensive regulatory information for "Biumoni" respirator in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number f5010d8d27f480ff58d70349eedc9035 and manufactured by CAREFUSION. The authorized representative in Taiwan is BIOSYSTEMS 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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f5010d8d27f480ff58d70349eedc9035
Registration Details
Taiwan FDA Registration: f5010d8d27f480ff58d70349eedc9035
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Device Details

"Biumoni" respirator
TW: โ€œๅธƒ่Žซๅฐผโ€ๅ‘ผๅธๅ™จ
Risk Class 2
Cancelled

Registration Details

f5010d8d27f480ff58d70349eedc9035

DHA00601831100

Company Information

United States

Product Details

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

D Anesthesiology

D.5895 Continuous respirators

import

Dates and Status

Sep 06, 2007

Sep 06, 2017

Nov 15, 2019

Cancellation Information

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