Taiwan FDA registration 90f1413a24b19d26190fd4ded8dc3b9f
Intensive care patient monitors
TW: 重症病患監護器
Taiwan·KONE OY INSTRUMENT DIVISION·Registered Jun 09, 1982 – Jun 09, 1987CancelledRegistration details
- Analysis ID
- 90f1413a24b19d26190fd4ded8dc3b9f
- Customs Code
- DHA00600207106
Company information
- Manufacturer
- KONE OY INSTRUMENT DIVISION
- Manufacturer Country
- Finland
- Authorized Representative
- West River International Co., Ltd
Product details
- Product Type (Level 1)
- 0601 Intensive Care Unit and Cardiac Intensive Care Unit Equipment
- Import Information
- import
Dates and status
- Registration Date
- Jun 09, 1982
- Expiry Date
- Jun 09, 1987
- Cancellation Date
- Mar 05, 1988
Cancellation information
- Status
- Logged out
- Reason
- 有效期間已屆未能補件
About this record
Access comprehensive regulatory information for Intensive care patient monitors in Taiwan's medical device market through Pure Global AI's free database. is registered under number 90f1413a24b19d26190fd4ded8dc3b9f and manufactured by KONE OY INSTRUMENT DIVISION. The authorized representative in Taiwan is West River International 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