"Kodak" digital X-ray system
Taiwan·Risk Class 2·CARESTREAM HEALTH,INC. EQUIPMENT DEVELOPMENT AND MANUFACTURING·Registered Jul 11, 2008 – Jul 11, 2013Cancelled- Analysis ID
- 8bca1ac24994fa612f3c451c97d0642c
- Customs Code
- DHAS0601910800
- Manufacturer Country
- United States
- Authorized Representative
- Taiwan Kangshi Medical Equipment 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
- Consent must be attached to the import (with the consent of the Atomic Energy Commission must be obtained for each import); input
- Registration Date
- Jul 11, 2008
- Expiry Date
- Jul 11, 2013
- Cancellation Date
- Apr 09, 2015
- Status
- Logged out
- Reason
- 許可證已逾有效期
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Access comprehensive regulatory information for "Kodak" digital X-ray system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 8bca1ac24994fa612f3c451c97d0642c and manufactured by CARESTREAM HEALTH,INC. EQUIPMENT DEVELOPMENT AND MANUFACTURING. The authorized representative in Taiwan is Taiwan Kangshi Medical Equipment Co., Ltd.
This page provides complete technical specifications, regulatory compliance details, 3 companies making similar products including RAYCO (SHANGHAI) MEDICAL PRODUCTS COMPANY LIMITED, RAYCO(SHANGHAI) MEDICAL PRODUCTS COMPANY LIMITED, and 3 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.