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"Leishi" oxygen mask (unsterilized)  - Taiwan Registration 80b88c1d48ab7aaba068d9cd01cdd553

Access comprehensive regulatory information for "Leishi" oxygen mask (unsterilized)  in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 80b88c1d48ab7aaba068d9cd01cdd553 and manufactured by RESPIRONICS MEDICAL PRODUCTS (SZ) CO., LTD.. The authorized representative in Taiwan is PHILIPS TAIWAN LIMITED.

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including RESPIRONICS, INC., and 1 recent registrations in the same category. 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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80b88c1d48ab7aaba068d9cd01cdd553
Registration Details
Taiwan FDA Registration: 80b88c1d48ab7aaba068d9cd01cdd553
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Device Details

"Leishi" oxygen mask (unsterilized) 
TW: “磊仕”氧氣面罩(未滅菌) 
Risk Class 1
Cancelled

Registration Details

80b88c1d48ab7aaba068d9cd01cdd553

DHA04600109308

Company Information

Product Details

Limited to the first level identification scope of the Measures for the Administration of Medical Devices "Oxygen Mask (D.5580)".

D Anesthesiology

D.5580 Oxygen masks

Input;; Chinese goods

Dates and Status

Oct 12, 2010

Oct 12, 2020

Dec 04, 2019

Cancellation Information

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