Taiwan FDA registration 3d029e22ca34177647eee8fb58cefe8d
“RESMED” BILEVEL POSITIVE PRESSURE SYSTEM
TW: “瑞思邁”雙陽壓呼吸輔助系統
Taiwan·Risk Class 2·MD·RESMED LTD·Registered Feb 26, 2015 – Feb 26, 2020CancelledRegistration details
- Analysis ID
- 3d029e22ca34177647eee8fb58cefe8d
- License Form
- Ministry of Health Medical Device Import No. 027029
- Customs Code
- DHA05602702901
Company information
- Manufacturer
- RESMED LTD
- Manufacturer Country
- Australia
- Authorized Representative
- BROJAW INC.
Product details
- 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
- Feb 26, 2015
- Expiry Date
- Feb 26, 2020
- Cancellation Date
- Aug 05, 2022
Cancellation information
- Status
- Logged out
- Reason
- 未展延而逾期者
About this record
Access comprehensive regulatory information for “RESMED” BILEVEL POSITIVE PRESSURE SYSTEM in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 3d029e22ca34177647eee8fb58cefe8d and manufactured by RESMED LTD. The authorized representative in Taiwan is BROJAW INC..
This page provides complete technical specifications, regulatory compliance details. 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+ Devices