Taiwan FDA registration 81ced1e7db43d3f0a8fac2f8c6a6c2f4
"Wellen" handheld vision refractive machine (unsterilized)
TW: "韋倫" 手持式視力驗光機 (未滅菌)
Taiwan·Risk Class 1·WELCH ALLYN INC.·Registered Dec 29, 2015 – Dec 29, 2020CancelledRegistration details
- Analysis ID
- 81ced1e7db43d3f0a8fac2f8c6a6c2f4
- Customs Code
- DHA09401602907
Company information
- Manufacturer
- WELCH ALLYN INC.
- Manufacturer Country
- United States
- Authorized Representative
- JAG MEDICAL CO., LTD.
Product details
- Intended Use
- Limited to the first level recognition range of ophthalmic optometry machine (M.1760) of the management measures for medical equipment.
- Product Type (Level 1)
- M Ophthalmology
- Product Type (Level 2)
- M.1760 Automatic Ophthalmic Optical Machine
- Import Information
- Input;; QMS/QSD
Dates and status
- Registration Date
- Dec 29, 2015
- Expiry Date
- Dec 29, 2020
- Cancellation Date
- Jun 07, 2022
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Wellen" handheld vision refractive machine (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 81ced1e7db43d3f0a8fac2f8c6a6c2f4 and manufactured by WELCH ALLYN INC.. The authorized representative in Taiwan is JAG MEDICAL CO., LTD..
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