Taiwan FDA registration 49d59ba8ddbe969f7e554be78fc29650
"Heidelberg" retinal imaging diagnostic system
TW: “海德堡”視網膜影像診斷系統
Taiwan·Risk Class 2·HEIDELBERG ENGINEERING GMBH·Registered Jan 22, 2010 – Jan 22, 2015CancelledRegistration details
- Analysis ID
- 49d59ba8ddbe969f7e554be78fc29650
- Customs Code
- DHA00602055007
Company information
- Manufacturer
- HEIDELBERG ENGINEERING GMBH
- Manufacturer Country
- Germany
- Authorized Representative
- TAIWAN HWA IN ENTERPRISE CO., LTD.
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- M Ophthalmology
- Product Type (Level 2)
- M.1570 Fundus Mirrors
- Import Information
- import
Dates and status
- Registration Date
- Jan 22, 2010
- Expiry Date
- Jan 22, 2015
- Cancellation Date
- Jun 26, 2018
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Heidelberg" retinal imaging diagnostic system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 49d59ba8ddbe969f7e554be78fc29650 and manufactured by HEIDELBERG ENGINEERING GMBH. The authorized representative in Taiwan is TAIWAN HWA IN ENTERPRISE CO., LTD..
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