Taiwan FDA registration cc879cd80d925cd1aa97884060e93f12
"Joy" developer and fixer (unsterilized)
TW: "喜悅"顯影液與定影液(未滅菌)
Taiwan·Risk Class 1·AGFA HEALTHCARE N. V.·Registered Mar 13, 2006 – Mar 13, 2016CancelledRegistration details
- Analysis ID
- cc879cd80d925cd1aa97884060e93f12
- Customs Code
- DHA04400290000
Company information
- Manufacturer
- AGFA HEALTHCARE N. V.
- Manufacturer Country
- Belgium
- Authorized Representative
- Taiwan Agfa Medical Equipment Co., Ltd
Product details
- Intended Use
- Liquids for the processing of radiographic films.
- Product Type (Level 1)
- P Radiology Science
- Product Type (Level 2)
- P.1840 Radiographic film
- Import Information
- import
Dates and status
- Registration Date
- Mar 13, 2006
- Expiry Date
- Mar 13, 2016
- Cancellation Date
- Apr 25, 2018
Cancellation information
- Status
- Logged out
- Reason
- 自行鍵入
About this record
Access comprehensive regulatory information for "Joy" developer and fixer (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number cc879cd80d925cd1aa97884060e93f12 and manufactured by AGFA HEALTHCARE N. V.. The authorized representative in Taiwan is Taiwan Agfa Medical Equipment Co., Ltd.
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