Taiwan FDA registration 80b88c1d48ab7aaba068d9cd01cdd553

"Leishi" oxygen mask (unsterilized) 

TW: “磊仕”氧氣面罩(未滅菌) 
Taiwan flagTaiwan·Risk Class 1·RESPIRONICS MEDICAL PRODUCTS (SZ) CO., LTD.·Registered Oct 12, 2010 – Oct 12, 2020Cancelled
Registration details
Analysis ID
80b88c1d48ab7aaba068d9cd01cdd553
Customs Code
DHA04600109308
Company information
Manufacturer Country
China
Authorized Representative
PHILIPS TAIWAN LIMITED
Product details
Intended Use
Limited to the first level identification scope of the Measures for the Administration of Medical Devices "Oxygen Mask (D.5580)".
Product Type (Level 1)
D Anesthesiology
Product Type (Level 2)
D.5580 Oxygen masks
Import Information
Input;; Chinese goods
Dates and status
Registration Date
Oct 12, 2010
Expiry Date
Oct 12, 2020
Cancellation Date
Dec 04, 2019
Cancellation information
Status
Logged out
Reason
自行鍵入
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About this record

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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