Taiwan FDA registration 847777028dce5bcb61a49fe18a73f6f3
"Heini" retinal scope and its accessories (unsterilized)
TW: "海尼" 視網膜鏡及其附件 (未滅菌)
Taiwan·Risk Class 1·HEINE OPTOTECHNIK GMBH & CO. LTD.·Registered Apr 28, 2006 – Apr 28, 2011CancelledRegistration details
- Analysis ID
- 847777028dce5bcb61a49fe18a73f6f3
- Customs Code
- DHA04400427003
Company information
- Manufacturer
- HEINE OPTOTECHNIK GMBH & CO. LTD.
- Manufacturer Country
- Germany
- Authorized Representative
- Meidcheng Instrument Co., Ltd
Product details
- Product Type (Level 1)
- M Ophthalmology
- Product Type (Level 2)
- M.1780 Retinal Lens
- Import Information
- import
Dates and status
- Registration Date
- Apr 28, 2006
- Expiry Date
- Apr 28, 2011
- Cancellation Date
- Aug 18, 2006
Cancellation information
- Status
- Logged out
- Reason
- 依藥事法第97條規定
About this record
Access comprehensive regulatory information for "Heini" retinal scope and its accessories (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 847777028dce5bcb61a49fe18a73f6f3 and manufactured by HEINE OPTOTECHNIK GMBH & CO. LTD.. The authorized representative in Taiwan is Meidcheng Instrument Co., Ltd.
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