Taiwan FDA registration d1bf4cf28c73966b3fc4ebb810cc82cc
"Ashi" Manual Eye Surgery Instruments (Unsterilized)
TW: “雅視”手動式眼科手術器械 (未滅菌)
Taiwan·Risk Class 1·RZ MEDIZINTECHNIK GMBH·Registered May 22, 2009 – May 22, 2014CancelledRegistration details
- Analysis ID
- d1bf4cf28c73966b3fc4ebb810cc82cc
- Customs Code
- DHA04400774908
Company information
- Manufacturer
- RZ MEDIZINTECHNIK GMBH
- Manufacturer Country
- Germany
- Authorized Representative
- Shanghua Industrial 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
- May 22, 2009
- Expiry Date
- May 22, 2014
- Cancellation Date
- Dec 14, 2016
Cancellation information
- Status
- Logged out
- Reason
- 屆期未申請展延
About this record
Access comprehensive regulatory information for "Ashi" 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 d1bf4cf28c73966b3fc4ebb810cc82cc and manufactured by RZ MEDIZINTECHNIK GMBH. The authorized representative in Taiwan is Shanghua Industrial Co., Ltd.
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