Taiwan FDA registration 094d7bcc1e12af3c49acfbbfe3a5bdd8
"Heini" fiber optic ophthalmic projector (unsterilized)
TW: “海尼”光纖眼科用投影機 (未滅菌)
Taiwan·Risk Class 1·HEINE OPTOTECHNIK GMBH & CO. LTD.·Registered Jul 06, 2007 – Jul 06, 2012CancelledRegistration details
- Analysis ID
- 094d7bcc1e12af3c49acfbbfe3a5bdd8
- Customs Code
- DHA04400598500
Company information
- Manufacturer
- HEINE OPTOTECHNIK GMBH & CO. LTD.
- Manufacturer Country
- Germany
- Authorized Representative
- Poussen Industrial Limited
Product details
- Intended Use
- Limited to the first level recognition range of ophthalmic projectors (M.1680) for the management of medical equipment.
- Product Type (Level 1)
- M Ophthalmology
- Product Type (Level 2)
- M.1680 眼科用投影機
- Import Information
- import
Dates and status
- Registration Date
- Jul 06, 2007
- Expiry Date
- Jul 06, 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" fiber optic ophthalmic projector (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 094d7bcc1e12af3c49acfbbfe3a5bdd8 and manufactured by HEINE OPTOTECHNIK GMBH & CO. LTD.. The authorized representative in Taiwan is Poussen Industrial Limited.
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