"Konica Minolta" dry laser (unsterilized)
Taiwan·Risk Class 1·KONICA MINOLTA MEDICAL & GRAPHIC, INC.·Registered May 08, 2007 – May 08, 2012Cancelled- Analysis ID
- ce6e86d9d6d0b2809c93e23c915656c7
- Customs Code
- DHA04400583201
- Manufacturer
- KONICA MINOLTA MEDICAL & GRAPHIC, INC.
- Manufacturer Country
- Japan
- Authorized Representative
- MEDEPOCH TRADING CO., LTD.
- Intended Use
- Limited to the first level identification range of the Measures for the Administration of Medical Devices "Radiographic Film (P.1840)".
- Product Type (Level 1)
- P Radiology Science
- Product Type (Level 2)
- P.1840 Radiographic film
- Import Information
- import
- Registration Date
- May 08, 2007
- Expiry Date
- May 08, 2012
- Cancellation Date
- May 05, 2014
- Status
- Logged out
- Reason
- 許可證已逾有效期
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Access comprehensive regulatory information for "Konica Minolta" dry laser (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number ce6e86d9d6d0b2809c93e23c915656c7 and manufactured by KONICA MINOLTA MEDICAL & GRAPHIC, INC.. 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 MEDICAL & GRAPHIC, INC., and 2 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.