Taiwan FDA registration 7bd11343ce6b5707fe13c835ae03e200
"Agfa" film (unsterilized)
TW: “愛克發” 軟片（未滅菌）
Taiwan·Risk Class 1·AGFA HEALTHCARE N. V.;; AGFA-GEVAERT N.V.·Registered Nov 21, 2005 – Nov 21, 2015CancelledRegistration details
- Analysis ID
- 7bd11343ce6b5707fe13c835ae03e200
- Customs Code
- DHA04400205107
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
- Images can be recorded during diagnostic radiology.
- Product Type (Level 1)
- P Radiology Science
- Product Type (Level 2)
- P.1840 Radiographic film
- Import Information
- import
Dates and status
- Registration Date
- Nov 21, 2005
- Expiry Date
- Nov 21, 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" film (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 7bd11343ce6b5707fe13c835ae03e200 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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