Taiwan FDA registration b81222e4a4e858307037a76d99c54073

"Kariki" General surgical instrument (unsterilized)

TW: "格利希" 一般手術用器械(未滅菌)

Taiwan·Risk Class 1·QURESHI MANUFACTURING CORPORATION·Registered Mar 31, 2006 – Mar 31, 2026Expired

Registration details

Analysis ID: b81222e4a4e858307037a76d99c54073
Customs Code: DHA04400339607

Company information

Manufacturer: QURESHI MANUFACTURING CORPORATION
Manufacturer Country: Pakistan
Authorized Representative: AK INSTRUMENTS CO., LTD.

Product details

Intended Use: Limited to the first level identification scope of the "Manual Instruments for General Surgery (I.4800)" of the Measures for the Classification and Grading Management of Medical Equipment.
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: Mar 31, 2006
Expiry Date: Mar 31, 2026

About this record

Access comprehensive regulatory information for "Kariki" General 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 b81222e4a4e858307037a76d99c54073 and manufactured by QURESHI MANUFACTURING CORPORATION. The authorized representative in Taiwan is AK INSTRUMENTS CO., LTD..

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