Taiwan FDA registration bee3a47029d19974bf164bdc4c8ae9c0
"Heidelberg" cataract and refractive imaging diagnostic platform
TW: “海德堡”白內障及屈光影像診斷平台
Taiwan·Risk Class 2·HEIDELBERG ENGINEERING GMBH·Registered Oct 31, 2019 – Oct 31, 2029ActiveRegistration details
- Analysis ID
- bee3a47029d19974bf164bdc4c8ae9c0
- Customs Code
- DHA05603291007
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
- Oct 31, 2019
- Expiry Date
- Oct 31, 2029
About this record
Access comprehensive regulatory information for "Heidelberg" cataract and refractive imaging diagnostic platform in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number bee3a47029d19974bf164bdc4c8ae9c0 and manufactured by HEIDELBERG ENGINEERING GMBH. The authorized representative in Taiwan is TAIWAN HWA IN ENTERPRISE CO., LTD..
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