Taiwan FDA registration 66d9f2e9d2a80ebfc054fd7933535df5
"Kodak" full-port digital X-ray system
TW: “柯達”全口數位X光系統
Taiwan·Risk Class 2·TROPHY·Registered Apr 09, 2009 – Apr 09, 2014CancelledRegistration details
- Analysis ID
- 66d9f2e9d2a80ebfc054fd7933535df5
- Customs Code
- DHAS0601977207
Company information
- Manufacturer
- TROPHY
- Manufacturer Country
- France
- Authorized Representative
- Taiwan Kangshi Medical Equipment Co., Ltd
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order.
- Product Type (Level 1)
- F Dentistry
- Product Type (Level 2)
- F.1800 口腔外X光照射系統
- Import Information
- Input;; Consent letter must be attached to the import (consent from the Atomic Energy Commission must be obtained for each import)
Dates and status
- Registration Date
- Apr 09, 2009
- Expiry Date
- Apr 09, 2014
- Cancellation Date
- Jan 09, 2017
Cancellation information
- Status
- Logged out
- Reason
- 自行鍵入
About this record
Access comprehensive regulatory information for "Kodak" full-port 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 66d9f2e9d2a80ebfc054fd7933535df5 and manufactured by TROPHY. The authorized representative in Taiwan is Taiwan Kangshi Medical Equipment 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