Taiwan FDA registration e2deaae74b746a8e543a31db24820728

“ResMed” Bilevel Positive Airway Pressure Device

TW: “瑞思邁”雙氣道正壓呼吸輔助器
Taiwan flagTaiwan·Risk Class 2·MD·ResMed Pty Ltd·Registered Jan 05, 2017 – Jan 05, 2027Active
Registration details
Analysis ID
e2deaae74b746a8e543a31db24820728
License Form
Ministry of Health Medical Device Import No. 029265
Customs Code
DHA05602926507
Company information
Manufacturer
ResMed Pty Ltd
Manufacturer Country
Australia
Authorized Representative
RESMED TAIWAN CO., LTD.
Product details
Intended Use
For details, it is Chinese approved copy of the imitation order
Product Type (Level 1)
D Devices for anesthesiology
Product Type (Level 2)
D5895 Continuous breathing apparatus
Import Information
Imported from abroad
Dates and status
Registration Date
Jan 05, 2017
Expiry Date
Jan 05, 2027
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About this record

Access comprehensive regulatory information for “ResMed” Bilevel Positive Airway Pressure Device in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number e2deaae74b746a8e543a31db24820728 and manufactured by ResMed Pty Ltd. The authorized representative in Taiwan is RESMED TAIWAN CO., LTD..

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including ResMed Pty 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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