Taiwan FDA registration 716f1d3d20b657e10f336b11a7ad8171
"Bidi" eye scalpel (sterilized)
TW: "必帝"眼科手術刀(滅菌)
Taiwan·Risk Class 1·BD OPHTHALMIC SYSTEMS·Registered Apr 17, 2006 – Apr 17, 2011CancelledRegistration details
- Analysis ID
- 716f1d3d20b657e10f336b11a7ad8171
- Customs Code
- DHA04400400000
Company information
- Manufacturer
- BD OPHTHALMIC SYSTEMS
- Manufacturer Country
- United Kingdom
- Authorized Representative
- BOULDER 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
- Input;; QMS/QSD
Dates and status
- Registration Date
- Apr 17, 2006
- Expiry Date
- Apr 17, 2011
- Cancellation Date
- Nov 09, 2012
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Bidi" eye scalpel (sterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 716f1d3d20b657e10f336b11a7ad8171 and manufactured by BD OPHTHALMIC SYSTEMS. The authorized representative in Taiwan is BOULDER ENTERPRISE CO., LTD..
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