Taiwan FDA registration dabcd1cab003d5c49f87371f68b44a3a
"Io" Manual Ophthalmic Surgical Instruments (Unsterilized)
TW: “艾歐” 手動式眼科手術器械(未滅菌)
Taiwan·Risk Class 1·AMERICAN OPTISURGICAL INC.·Registered Oct 25, 2010 – Oct 25, 2015CancelledRegistration details
- Analysis ID
- dabcd1cab003d5c49f87371f68b44a3a
- Customs Code
- DHA04400939700
Company information
- Manufacturer
- AMERICAN OPTISURGICAL INC.
- Manufacturer Country
- United States
- Authorized Representative
- RAY HUNG INSTRUMENT CO., LTD.
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
- Oct 25, 2010
- Expiry Date
- Oct 25, 2015
- Cancellation Date
- Jun 28, 2018
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Io" Manual Ophthalmic Surgical Instruments (Unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number dabcd1cab003d5c49f87371f68b44a3a and manufactured by AMERICAN OPTISURGICAL INC.. The authorized representative in Taiwan is RAY HUNG INSTRUMENT CO., LTD..
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