Taiwan FDA registration 36a3aeafe3dbf594c94a31a977b7958b

“ResMed” POSITIVE AIRWAY PRESSURE THERAPY DEVICE

TW: “瑞思邁”雙氣道正壓呼吸治療器
Taiwan flagTaiwan·Risk Class 2·MD·RESMED LIMITED·Registered Jul 12, 2017 – Jul 12, 2022Expired
Registration details
Analysis ID
36a3aeafe3dbf594c94a31a977b7958b
License Form
Ministry of Health Medical Device Import No. 029967
Customs Code
DHA05602996700
Company information
Manufacturer
RESMED LIMITED
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
Jul 12, 2017
Expiry Date
Jul 12, 2022
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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 36a3aeafe3dbf594c94a31a977b7958b and manufactured by RESMED LIMITED. 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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