Taiwan FDA registration d3b0f51243c850e6eae43de813a286e5
"Anbi" surgical instrument (unsterilized)
TW: “安美”外科器械 (未滅菌)
Taiwan·Risk Class 1·AEMCO Z.E (PVT) LTD.·Registered Nov 03, 2008 – Nov 03, 2018CancelledRegistration details
- Analysis ID
- d3b0f51243c850e6eae43de813a286e5
- Customs Code
- DHA04400722003
Company information
- Manufacturer
- AEMCO Z.E (PVT) LTD.
- Manufacturer Country
- Pakistan
- Authorized Representative
- MEDLINE TAIWAN COMPANY LIMITED
Product details
- Intended Use
- Limited to the first level identification scope of the Measures for the Administration of Medical Devices "Manual Instruments for General Surgery (I.4800)".
- Product Type (Level 1)
- I General, Plastic Surgery and Dermatology
- Product Type (Level 2)
- I.4800 Hand Instruments for General Surgery
- Import Information
- import
Dates and status
- Registration Date
- Nov 03, 2008
- Expiry Date
- Nov 03, 2018
- Cancellation Date
- Jan 17, 2022
Cancellation information
- Status
- Logged out
- Reason
- 屆期未申請展延;;自請註銷
About this record
Access comprehensive regulatory information for "Anbi" surgical instrument (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number d3b0f51243c850e6eae43de813a286e5 and manufactured by AEMCO Z.E (PVT) LTD.. The authorized representative in Taiwan is MEDLINE TAIWAN COMPANY LIMITED.
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