Taiwan FDA registration 98cd8f51efb6119678032550a6b694f7
"Heidelberg" keratoscope (unsterilized)
TW: “海德堡”角膜鏡 (未滅菌)
Taiwan·Risk Class 1·HEIDELBERG ENGINEERING GMBH·Registered Aug 24, 2009 – Aug 24, 2014CancelledRegistration details
- Analysis ID
- 98cd8f51efb6119678032550a6b694f7
- Customs Code
- DHA04400798102
Company information
- Manufacturer
- HEIDELBERG ENGINEERING GMBH
- Manufacturer Country
- Germany
- Authorized Representative
- TAIWAN HWA IN ENTERPRISE CO., LTD.
Product details
- Intended Use
- Limited to the first level identification range of the "Corneatoscope (M.1350)" of the Measures for the Administration of Medical Devices.
- Product Type (Level 1)
- M Ophthalmology
- Product Type (Level 2)
- M.1350 Coratoscope
- Import Information
- import
Dates and status
- Registration Date
- Aug 24, 2009
- Expiry Date
- Aug 24, 2014
- 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" keratoscope (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 98cd8f51efb6119678032550a6b694f7 and manufactured by HEIDELBERG ENGINEERING GMBH. The authorized representative in Taiwan is TAIWAN HWA IN ENTERPRISE CO., LTD..
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