Taiwan FDA registration 3ba66a5834c561389ad44f496674b794
"Heidelberg" foreroom optical tomography
TW: “海德堡”前房光學斷層掃描儀
Taiwan·Risk Class 2·HEIDELBERG ENGINEERING GMBH·Registered May 04, 2010 – May 04, 2015CancelledRegistration details
- Analysis ID
- 3ba66a5834c561389ad44f496674b794
- Customs Code
- DHA00602094606
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.1850 交流電力式細隙燈
- Import Information
- import
Dates and status
- Registration Date
- May 04, 2010
- Expiry Date
- May 04, 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" foreroom optical tomography in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 3ba66a5834c561389ad44f496674b794 and manufactured by HEIDELBERG ENGINEERING GMBH. The authorized representative in Taiwan is TAIWAN HWA IN ENTERPRISE CO., LTD..
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