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"Leishi" bronchial examination elbow - Taiwan Registration d09bcb19f8853baab9d96d3e752ccd46

Access comprehensive regulatory information for "Leishi" bronchial examination elbow in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number d09bcb19f8853baab9d96d3e752ccd46 and manufactured by RESPIRONICS INC.. The authorized representative in Taiwan is PHILIPS TAIWAN LIMITED.

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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d09bcb19f8853baab9d96d3e752ccd46
Registration Details
Taiwan FDA Registration: d09bcb19f8853baab9d96d3e752ccd46
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Device Details

"Leishi" bronchial examination elbow
TW: โ€œ็ฃŠไป•โ€ๆ”ฏๆฐฃ็ฎกๆชขๆŸฅๅฝŽ็ฎก
Risk Class 2

Registration Details

d09bcb19f8853baab9d96d3e752ccd46

DHA00602413706

Company Information

United States

Product Details

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

D Anesthesiology

D.5905 Non-continuous respirators

import

Dates and Status

Oct 17, 2012

Oct 17, 2027