Taiwan FDA registration a2f6f855d0b5a3b803f5cd69b422d602
"Daejeon" vision tester (unsterilized)
TW: “大田”視力檢查器（未滅菌）
Taiwan·Risk Class 1·HUNG YI MEDICAL INSTRUMENT CO., LTD.·Registered Dec 11, 2012 – Dec 11, 2017CancelledRegistration details
- Analysis ID
- a2f6f855d0b5a3b803f5cd69b422d602
Company information
- Manufacturer
- HUNG YI MEDICAL INSTRUMENT CO., LTD.
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- EZ-CARE INSTRUMENTS. CO., LTD.
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
- Contract manufacturing;; Domestic
Dates and status
- Registration Date
- Dec 11, 2012
- Expiry Date
- Dec 11, 2017
- Cancellation Date
- Dec 13, 2019
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Daejeon" vision tester (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number a2f6f855d0b5a3b803f5cd69b422d602 and manufactured by HUNG YI MEDICAL INSTRUMENT CO., LTD.. The authorized representative in Taiwan is EZ-CARE INSTRUMENTS. CO., LTD..
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