Taiwan FDA registration 42799fdf0ed8d00b7e2609e4533d0c42
Mobile multifunctional ECG system
TW: 移動式多功能心電圖系統
Registration details
- Analysis ID
- 42799fdf0ed8d00b7e2609e4533d0c42
- Customs Code
- DHA00600419100
Company information
- Manufacturer
- QUINTON INSTRUMENT CO.
- Manufacturer Country
- United States
- Authorized Representative
- Tiandi Trading Co., Ltd
Product details
- Product Type (Level 1)
- 0801 Electrocardiograph
- Import Information
- import
Dates and status
- Registration Date
- Mar 22, 1986
- Expiry Date
- Mar 22, 1991
- Cancellation Date
- Oct 05, 1999
Cancellation information
- Status
- Logged out
- Reason
- 改列無須辦理查驗之醫療器材;;未展延而逾期者
About this record
Access comprehensive regulatory information for Mobile multifunctional ECG system in Taiwan's medical device market through Pure Global AI's free database. is registered under number 42799fdf0ed8d00b7e2609e4533d0c42 and manufactured by QUINTON INSTRUMENT CO.. The authorized representative in Taiwan is Tiandi Trading 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