Taiwan FDA registration 67437cb65f0de51175bf5708043471cc
AeroChamber Vent Chamber
TW: 愛治喘噴藥輔助器
Registration details
- Analysis ID
- 67437cb65f0de51175bf5708043471cc
- License Form
- Ministry of Health Medical Device Import No. 029651
- Customs Code
- DHA05602965102
Company information
- Manufacturer
- MONAGHAN MEDICAL CORP.
- Manufacturer Country
- United States
- 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 Devices for anesthesiology
- Product Type (Level 2)
- D5630 Sprayer
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Apr 05, 2017
- Expiry Date
- Apr 05, 2022
About this record
Access comprehensive regulatory information for AeroChamber Vent Chamber in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 67437cb65f0de51175bf5708043471cc and manufactured by MONAGHAN MEDICAL CORP.. 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