"Konica Minolta" medical imaging digitizer
- Analysis ID
- 869821382f1ec119c5b2644d3ad9e8fc
- Customs Code
- DHA00602283000
- Manufacturer
- KONICA MINOLTA TECHNOPRODUCTS CO., LTD.
- Manufacturer Country
- Japan
- Authorized Representative
- MEDEPOCH TRADING CO., LTD.
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- P Radiology Science
- Product Type (Level 2)
- P.1650 透視X光影像增感管
- Import Information
- import
- Registration Date
- Oct 03, 2011
- Expiry Date
- Oct 03, 2016
- Cancellation Date
- Aug 21, 2018
- Status
- Logged out
- Reason
- 未展延而逾期者
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Access comprehensive regulatory information for "Konica Minolta" medical imaging digitizer in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 869821382f1ec119c5b2644d3ad9e8fc and manufactured by KONICA MINOLTA TECHNOPRODUCTS CO., LTD.. The authorized representative in Taiwan is MEDEPOCH TRADING CO., LTD..
This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including KONICA MINOLTA TECHNOPRODUCTS CO., LTD., and 5 recent registrations in the same category. 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.