Taiwan FDA registration b5b7bbe04445ad186aa3407102e67ec1
“AIRSEP” NewLife Intensity Oxygen Concentrator
TW: “亞適”氧氣濃縮機
Taiwan·Risk Class 2·MD·Caire Inc.·Registered Jun 14, 2017 – Jun 14, 2027ActiveRegistration details
- Analysis ID
- b5b7bbe04445ad186aa3407102e67ec1
- License Form
- Ministry of Health Medical Device Import No. 029790
- Customs Code
- DHA05602979000
Company information
- Manufacturer
- Caire Inc.
- Manufacturer Country
- United States
- Authorized Representative
- BESMED HEALTH BUSINESS CORP.
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)
- D5440 portable oxygen generator
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Jun 14, 2017
- Expiry Date
- Jun 14, 2027
About this record
Access comprehensive regulatory information for “AIRSEP” NewLife Intensity Oxygen Concentrator in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number b5b7bbe04445ad186aa3407102e67ec1 and manufactured by Caire Inc.. The authorized representative in Taiwan is BESMED HEALTH BUSINESS CORP..
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