Taiwan FDA registration 4b2daa77fd6ca02c8a3fd3ab51d7a860

“ResMed” Positive Airway Pressure Therapy Device

TW: “瑞思邁”氣道正壓呼吸治療系統
Taiwan flagTaiwan·Risk Class 2·MD·ResMed Pty Ltd·Registered Aug 01, 2016 – Aug 01, 2026Active
Registration details
Analysis ID
4b2daa77fd6ca02c8a3fd3ab51d7a860
License Form
Ministry of Health Medical Device Import No. 028649
Customs Code
DHA05602864907
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
Aug 01, 2016
Expiry Date
Aug 01, 2026
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About this record

Access comprehensive regulatory information for “ResMed” Positive Airway Pressure Therapy Device in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 4b2daa77fd6ca02c8a3fd3ab51d7a860 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 LIMITED, 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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