Taiwan FDA registration af98a8c19bc12844939a5a5194314272

"Leishi" oxygen mask (unsterilized) 

TW: “磊仕”氧氣面罩(未滅菌) 
Taiwan flagTaiwan·Risk Class 1·RESPIRONICS, INC.·Registered Oct 12, 2010 – Oct 12, 2020Cancelled
Registration details
Analysis ID
af98a8c19bc12844939a5a5194314272
Customs Code
DHA04400935905
Company information
Manufacturer
RESPIRONICS, INC.
Manufacturer Country
United States
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
import
Dates and status
Registration Date
Oct 12, 2010
Expiry Date
Oct 12, 2020
Cancellation Date
Aug 16, 2018
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 af98a8c19bc12844939a5a5194314272 and manufactured by RESPIRONICS, INC.. 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 MEDICAL PRODUCTS (SZ) CO., LTD., 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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