Taiwan FDA registration e29af16757f03c03201636d67a81a95e

"Jeli" manual instruments for general surgery (unsterilized)

TW: “傑立”一般手術用手動式器械 (未滅菌)

Taiwan·Risk Class 1·JEIL TECH CO., LTD.·Registered Jul 10, 2013 – Jul 10, 2018Cancelled

Registration details

Analysis ID: e29af16757f03c03201636d67a81a95e
Customs Code: DHA04401319707

Company information

Manufacturer: JEIL TECH CO., LTD.
Manufacturer Country: Korea, Republic of
Authorized Representative: LA MED INTERNATIONAL 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: import

Dates and status

Registration Date: Jul 10, 2013
Expiry Date: Jul 10, 2018
Cancellation Date: Aug 18, 2015

Cancellation information

Status: Logged out
Reason: 自請註銷

About this record

Access comprehensive regulatory information for "Jeli" manual instruments for general surgery (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number e29af16757f03c03201636d67a81a95e and manufactured by JEIL TECH CO., LTD.. The authorized representative in Taiwan is LA MED INTERNATIONAL CO., LTD..

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