Taiwan FDA registration 97306634f6360536921605a93019ad08
"Huai'an Aofu" manual eye surgery instruments (unsterilized)
TW: “淮安澳福”手動眼科手術器械(未滅菌)
Taiwan·Risk Class 1·HUAIAN WOLFRAM SURGICAL INSTRUMENTS CO., LTD.·Registered Apr 08, 2009 – Apr 08, 2019CancelledRegistration details
- Analysis ID
- 97306634f6360536921605a93019ad08
- Customs Code
- DHA04600065200
Company information
- Manufacturer
- HUAIAN WOLFRAM SURGICAL INSTRUMENTS CO., LTD.
- Manufacturer Country
- China
- Authorized Representative
- TAIWAN HWA IN ENTERPRISE 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
- Chinese goods;; input
Dates and status
- Registration Date
- Apr 08, 2009
- Expiry Date
- Apr 08, 2019
- Cancellation Date
- Jul 15, 2022
Cancellation information
- Status
- Logged out
- Reason
- 未展延而逾期者
About this record
Access comprehensive regulatory information for "Huai'an Aofu" manual eye surgery 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 97306634f6360536921605a93019ad08 and manufactured by HUAIAN WOLFRAM SURGICAL INSTRUMENTS CO., LTD.. The authorized representative in Taiwan is TAIWAN HWA IN ENTERPRISE CO., LTD..
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