Taiwan FDA registration 24df9bdaf30ac12a8e18d7da699b2d88
Automatic Revival Instrument 〝Security〞
TW: 自動甦醒器 〝安保〞
Registration details
- Analysis ID
- 24df9bdaf30ac12a8e18d7da699b2d88
- Customs Code
- DHA00600852602
Company information
- Manufacturer
- AMBU INTERNATIONAL A/S
- Manufacturer Country
- Denmark
- Authorized Representative
- Schmidt Technology Co., Ltd
Product details
- Product Type (Level 1)
- 0210 Cardiopulmonary awakener
- Import Information
- import
Dates and status
- Registration Date
- Jan 14, 1998
- Expiry Date
- Jan 14, 2003
- Cancellation Date
- Aug 28, 2007
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for Automatic Revival Instrument 〝Security〞 in Taiwan's medical device market through Pure Global AI's free database. is registered under number 24df9bdaf30ac12a8e18d7da699b2d88 and manufactured by AMBU INTERNATIONAL A/S. The authorized representative in Taiwan is Schmidt Technology 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