Taiwan FDA registration 2bfcf793fd834ad0a1f67e3912b71be2
“Philips” Cardiograph
TW: “飛利浦”心電圖儀
Taiwan·Risk Class 2·MD·PHILIPS MEDICAL SYSTEMS·Registered Mar 09, 2016 – Mar 09, 2021CancelledRegistration details
- Analysis ID
- 2bfcf793fd834ad0a1f67e3912b71be2
- License Form
- Ministry of Health Medical Device Import No. 028252
- Customs Code
- DHA05602825206
Company information
- Manufacturer
- PHILIPS MEDICAL SYSTEMS
- Manufacturer Country
- United States
- Authorized Representative
- PHILIPS TAIWAN LIMITED
Product details
- Product Type (Level 1)
- E Cardiovascular devices
- Product Type (Level 2)
- E2340 ECG Scanner
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Mar 09, 2016
- Expiry Date
- Mar 09, 2021
- Cancellation Date
- Sep 13, 2017
Cancellation information
- Status
- Logged out
- Reason
- 製造廠國別變更
About this record
Access comprehensive regulatory information for “Philips” Cardiograph in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 2bfcf793fd834ad0a1f67e3912b71be2 and manufactured by PHILIPS MEDICAL SYSTEMS. The authorized representative in Taiwan is PHILIPS TAIWAN 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