Taiwan FDA registration 51996567455e2388ba5ff0ee9e741ddc

“ResMed” AirFit Mask

TW: “瑞思邁” 易適面罩
Taiwan flagTaiwan·Risk Class 2·MD·ResMed Pty Ltd·Registered Jun 30, 2021 – Jun 30, 2026Expired
Registration details
Analysis ID
51996567455e2388ba5ff0ee9e741ddc
License Form
Ministry of Health Medical Device Import No. 034746
Customs Code
DHA05603474604
Company information
Manufacturer
ResMed Pty Ltd
Manufacturer Country
Australia
Authorized Representative
RESMED TAIWAN CO., LTD.
Product details
Intended Use
Details are as detailed as approved Chinese instructions
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
Jun 30, 2021
Expiry Date
Jun 30, 2026
Companies making similar products

Top companies providing products similar to "“ResMed” AirFit Mask"

Recent registrations

Recently registered similar products

About this record

Access comprehensive regulatory information for “ResMed” AirFit Mask in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 51996567455e2388ba5ff0ee9e741ddc 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.

Free DatabasePowered by Pure Global AI89,000+ Devices1 Competitors1 Recent Registrations