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Leishi anesthesia gas mask (unsterilized)  - Taiwan Registration bdf131818135bdaf29b0d6e9c5e93be1

Access comprehensive regulatory information for Leishi anesthesia gas 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 bdf131818135bdaf29b0d6e9c5e93be1 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, 2 companies making similar products including RCM MANUFACTURING INC. (RESPIRONICS PHILIPPINES), RESPIRONICS, INC., and 2 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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Registration Details
Taiwan FDA Registration: bdf131818135bdaf29b0d6e9c5e93be1
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Device Details

Leishi anesthesia gas mask (unsterilized) 
TW: “磊仕”麻醉氣體面罩 (未滅菌) 
Risk Class 1

Registration Details

bdf131818135bdaf29b0d6e9c5e93be1

DHA04600109206

Company Information

Product Details

Limited to the first level identification range of the "Anesthesia Gas Mask (D.5550)" of the Measures for the Classification and Grading Management of Medical Equipment.

D Anesthesiology

D.5550 麻醉氣體面罩

Chinese goods;; input

Dates and Status

Oct 12, 2010

Oct 12, 2025

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