Taiwan FDA registration 356ea7ea918b9c6952fd19f290670365
"Konica Minolta" blood oxygen saturation monitor
TW: “柯尼卡美能達”血氧飽和監測儀
Taiwan·Risk Class 2·KONICA MINOLTA SENSING, INC.·Registered Mar 30, 2007 – Mar 30, 2012CancelledRegistration details
- Analysis ID
- 356ea7ea918b9c6952fd19f290670365
- Customs Code
- DHA00601797503
Company information
- Manufacturer
- KONICA MINOLTA SENSING, INC.
- Manufacturer Country
- Japan
- Authorized Representative
- US CATSCAN TAIWAN LTD.
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.2700.
- Import Information
- import
Dates and status
- Registration Date
- Mar 30, 2007
- Expiry Date
- Mar 30, 2012
- Cancellation Date
- Nov 01, 2012
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Konica Minolta" blood oxygen saturation monitor in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 356ea7ea918b9c6952fd19f290670365 and manufactured by KONICA MINOLTA SENSING, INC.. The authorized representative in Taiwan is US CATSCAN TAIWAN 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