Taiwan FDA registration c255aae0f0ed0d6cd76cc38c72ed1e3f
"Suraku" ECG recorder
TW: "須樂"心電圖紀錄器
Taiwan·Risk Class 2·SCHILLER A.G.·Registered Jan 08, 2007 – Jan 08, 2012CancelledRegistration details
- Analysis ID
- c255aae0f0ed0d6cd76cc38c72ed1e3f
- Customs Code
- DHA00601766807
Company information
- Manufacturer
- SCHILLER A.G.
- Manufacturer Country
- Switzerland
- Authorized Representative
- Guanxuan Limited
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- E Cardiovascular Medicine Science
- Product Type (Level 2)
- E.2800 醫用磁帶記錄器
- Import Information
- import
Dates and status
- Registration Date
- Jan 08, 2007
- Expiry Date
- Jan 08, 2012
- Cancellation Date
- Apr 30, 2014
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Suraku" ECG recorder in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number c255aae0f0ed0d6cd76cc38c72ed1e3f and manufactured by SCHILLER A.G.. The authorized representative in Taiwan is Guanxuan Limited.
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