Taiwan FDA registration 7774b269e0df5b41c67738e89536c596
"Heidelberg" Streilly retinal imaging diagnostic system
TW: “海德堡” 史崔利視網膜影像診斷系統
Taiwan·Risk Class 2·HEIDELBERG ENGINEERING GMBH·Registered Jul 08, 2013 – Jul 08, 2028ActiveRegistration details
- Analysis ID
- 7774b269e0df5b41c67738e89536c596
- Customs Code
- DHA00602460207
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
- Jul 08, 2013
- Expiry Date
- Jul 08, 2028
About this record
Access comprehensive regulatory information for "Heidelberg" Streilly 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 7774b269e0df5b41c67738e89536c596 and manufactured by HEIDELBERG ENGINEERING GMBH. The authorized representative in Taiwan is TAIWAN HWA IN ENTERPRISE CO., LTD..
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