Taiwan FDA registration 8ad8b84b62f931c0964920f3c0d845d9

"Anjie" large bent basin (unsterilized)

TW: "安捷"大彎盆(未滅菌)

Taiwan·Risk Class 1·PACK & PROPER CO., LTD.·Registered Feb 01, 2012 – Feb 01, 2017Cancelled

Registration details

Analysis ID: 8ad8b84b62f931c0964920f3c0d845d9

Company information

Manufacturer: PACK & PROPER CO., LTD.
Manufacturer Country: Taiwan, Province of China
Authorized Representative: PACK & PROPER CO., LTD.

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: Domestic

Dates and status

Registration Date: Feb 01, 2012
Expiry Date: Feb 01, 2017
Cancellation Date: Dec 13, 2019

Cancellation information

Status: Logged out
Reason: 許可證已逾有效期

About this record

Access comprehensive regulatory information for "Anjie" large bent basin (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 8ad8b84b62f931c0964920f3c0d845d9 and manufactured by PACK & PROPER CO., LTD.. The authorized representative in Taiwan is PACK & PROPER CO., LTD..

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