Taiwan FDA registration 821883b24352fd3f3ee261d2690ab85c
"Agfa" developer and fixer (unsterilized)
TW: “愛克發” 顯影液與定影液（未滅菌）
Taiwan·Risk Class 1·AGFA HEALTHCARE N. V.;; AGFA-GEVAERT N.V.·Registered Dec 01, 2005 – Dec 01, 2015CancelledRegistration details
- Analysis ID
- 821883b24352fd3f3ee261d2690ab85c
- Customs Code
- DHA04400217601
Company information
- Manufacturer
- AGFA HEALTHCARE N. V.;; AGFA-GEVAERT 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
- Dec 01, 2005
- Expiry Date
- Dec 01, 2015
- Cancellation Date
- Apr 25, 2018
Cancellation information
- Status
- Logged out
- Reason
- 自行鍵入
About this record
Access comprehensive regulatory information for "Agfa" 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 821883b24352fd3f3ee261d2690ab85c and manufactured by AGFA HEALTHCARE N. V.;; AGFA-GEVAERT N.V.. The authorized representative in Taiwan is Taiwan Agfa Medical Equipment Co., Ltd.
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