Taiwan FDA registration bdf131818135bdaf29b0d6e9c5e93be1

Leishi anesthesia gas mask (unsterilized) 

TW: “磊仕”麻醉氣體面罩 (未滅菌) 
Taiwan flagTaiwan·Risk Class 1·RESPIRONICS MEDICAL PRODUCTS (SZ) CO., LTD.·Registered Oct 12, 2010 – Oct 12, 2025Expired
Registration details
Analysis ID
bdf131818135bdaf29b0d6e9c5e93be1
Customs Code
DHA04600109206
Company information
Manufacturer Country
China
Authorized Representative
PHILIPS TAIWAN LIMITED
Product details
Intended Use
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.
Product Type (Level 1)
D Anesthesiology
Product Type (Level 2)
D.5550 麻醉氣體面罩
Import Information
Chinese goods;; input
Dates and status
Registration Date
Oct 12, 2010
Expiry Date
Oct 12, 2025
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About this record

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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