Taiwan FDA registration 65ca3ec0d1e42fd9d1c5ecaca404ebc6
"Heini" battery-powered retinal scope and its accessories (unsterilized)
TW: “海尼”電池供電式視網膜鏡及其附件 (未滅菌)
Taiwan·Risk Class 1·HEINE OPTOTECHNIK GMBH & CO. KG·Registered Mar 22, 2007 – Mar 22, 2012CancelledRegistration details
- Analysis ID
- 65ca3ec0d1e42fd9d1c5ecaca404ebc6
- Customs Code
- DHA04400569004
Company information
- Manufacturer
- HEINE OPTOTECHNIK GMBH & CO. KG
- Manufacturer Country
- Germany
- Authorized Representative
- Poussen Industrial Limited
Product details
- Intended Use
- Limited to the first level recognition range of medical equipment management method retinal endoscopy (M.1780).
- Product Type (Level 1)
- M Ophthalmology
- Product Type (Level 2)
- M.1780 Retinal Lens
- Import Information
- Input;; QMS/QSD
Dates and status
- Registration Date
- Mar 22, 2007
- Expiry Date
- Mar 22, 2012
- Cancellation Date
- May 05, 2014
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Heini" battery-powered 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 65ca3ec0d1e42fd9d1c5ecaca404ebc6 and manufactured by HEINE OPTOTECHNIK GMBH & CO. KG. The authorized representative in Taiwan is Poussen Industrial Limited.
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