“RESMED” POSITIVE AIRWAY PRESSURE DEVICE
Taiwan·Risk Class 2·MD·RESMED LTD·Registered Apr 21, 2015 – Apr 21, 2020Cancelled- Analysis ID
- a757adf59b42e27e12e3f8d726d883ce
- License Form
- Ministry of Health Medical Device Import No. 027265
- Customs Code
- DHA05602726500
- Manufacturer
- RESMED LTD
- Manufacturer Country
- Australia
- Authorized Representative
- BROJAW INC.
- Product Type (Level 1)
- D Devices for anesthesiology
- Product Type (Level 2)
- D5895 Continuous breathing apparatus
- Import Information
- Imported from abroad
- Registration Date
- Apr 21, 2015
- Expiry Date
- Apr 21, 2020
- Cancellation Date
- Aug 05, 2022
- Status
- Logged out
- Reason
- 未展延而逾期者
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Access comprehensive regulatory information for “RESMED” 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 a757adf59b42e27e12e3f8d726d883ce and manufactured by RESMED LTD. The authorized representative in Taiwan is BROJAW INC..
This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including ResMed Pty Ltd., and 2 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.