Taiwan FDA registration 71fd945effc00a5ae9f6df335b9c57ed
Aiji breather aid
TW: 愛治喘吸藥輔助器
Registration details
- Analysis ID
- 71fd945effc00a5ae9f6df335b9c57ed
- Customs Code
- DHA00601135600
Company information
- Manufacturer
- Trudell Medical International
- Manufacturer Country
- Canada
- Authorized Representative
- STANDARD HEALTH MEDICAL CO., LTD.
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- D Anesthesiology
- Import Information
- import
Dates and status
- Registration Date
- Jun 02, 2005
- Expiry Date
- Jun 02, 2025
About this record
Access comprehensive regulatory information for Aiji breather aid in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 71fd945effc00a5ae9f6df335b9c57ed and manufactured by Trudell Medical International. The authorized representative in Taiwan is STANDARD HEALTH MEDICAL CO., LTD..
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