Taiwan FDA registration d9b6d1b2c1f66e3731576176a9dc0fbc
"Anton Meier" Guided Ophthalmology Manual Device (Unsterilized)
TW: “安東梅爾”視導眼科手動式器械(未滅菌)
Taiwan·Risk Class 1·ANTON MEYER & CO., LTD.·Registered Feb 12, 2007 – Feb 12, 2022CancelledRegistration details
- Analysis ID
- d9b6d1b2c1f66e3731576176a9dc0fbc
- Customs Code
- DHA04400560003
Company information
- Manufacturer
- ANTON MEYER & CO., LTD.
- Manufacturer Country
- Switzerland
- Authorized Representative
- BAUSCH & LOMB TAIWAN LIMITED
Product details
- Intended Use
- Limited to the first level identification scope of the Measures for the Administration of Medical Devices "Manual Eye Surgery Instruments (M.4350)".
- Product Type (Level 1)
- M Ophthalmology
- Product Type (Level 2)
- M.4350 手動式眼科手術器械
- Import Information
- import
Dates and status
- Registration Date
- Feb 12, 2007
- Expiry Date
- Feb 12, 2022
- Cancellation Date
- Apr 12, 2024
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Anton Meier" Guided Ophthalmology Manual Device (Unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number d9b6d1b2c1f66e3731576176a9dc0fbc and manufactured by ANTON MEYER & CO., LTD.. The authorized representative in Taiwan is BAUSCH & LOMB TAIWAN LIMITED.
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