Taiwan FDA registration fa2c9d2927826a46b716d05a35e8ddc2
Mobile multi-channel ECG recorder
TW: 移動式多頻道心電記錄器
Taiwan·QUINTON INSTRUMENT CO.·Registered May 24, 1988 – May 24, 1993CancelledRegistration details
- Analysis ID
- fa2c9d2927826a46b716d05a35e8ddc2
- Customs Code
- DHA00600519401
Company information
- Manufacturer
- QUINTON INSTRUMENT CO.
- Manufacturer Country
- United States
- Authorized Representative
- Pomei Enterprise Co., Ltd
Product details
- Product Type (Level 1)
- 0803 ECG recorder
- Import Information
- import
Dates and status
- Registration Date
- May 24, 1988
- Expiry Date
- May 24, 1993
- Cancellation Date
- Oct 06, 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 multi-channel ECG recorder in Taiwan's medical device market through Pure Global AI's free database. is registered under number fa2c9d2927826a46b716d05a35e8ddc2 and manufactured by QUINTON INSTRUMENT CO.. The authorized representative in Taiwan is Pomei Enterprise 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