Taiwan FDA registration 691338c89837b7bc87935a7b173ca76e
Pupillary manual refractive needle (unsterilized)
TW: 瞳光手動折射針(未滅菌)
Taiwan·Risk Class 1·SHANGHAI HUVITZ CO., LTD.·Registered May 29, 2012 – May 29, 2017CancelledRegistration details
- Analysis ID
- 691338c89837b7bc87935a7b173ca76e
- Customs Code
- DHA04600164702
Company information
- Manufacturer
- SHANGHAI HUVITZ CO., LTD.
- Manufacturer Country
- China
- Authorized Representative
- Mingda Development Company Limited
Product details
- Intended Use
- Limited to the first level identification range of the Measures for the Administration of Medical Devices "Manual Refractometer (M.1770)".
- Product Type (Level 1)
- M Ophthalmology
- Product Type (Level 2)
- M.1770 手動式驗光儀
- Import Information
- QMS/QSD;; Input;; Chinese goods
Dates and status
- Registration Date
- May 29, 2012
- Expiry Date
- May 29, 2017
- Cancellation Date
- Nov 29, 2017
Cancellation information
- Status
- Logged out
- Reason
- 公司歇業
About this record
Access comprehensive regulatory information for Pupillary manual refractive needle (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 691338c89837b7bc87935a7b173ca76e and manufactured by SHANGHAI HUVITZ CO., LTD.. The authorized representative in Taiwan is Mingda Development Company Limited.
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