Taiwan FDA registration 3404df8cb578c813da3857921cf45995

"Efinger" Manual surgical instrument for general use (Non-Sterile)

TW: "艾芬格" 一般手術用手動式器械 (未滅菌)

Taiwan·Risk Class 1·MD·EFINGER INSTRUMENTS GMBH & CO. KG·Registered Dec 22, 2016 – Dec 22, 2021Expired

Registration details

Analysis ID: 3404df8cb578c813da3857921cf45995
License Form: Ministry of Health Medical Device Import No. 017332
Customs Code: DHA09401733200

Company information

Manufacturer: EFINGER INSTRUMENTS GMBH & CO. KG
Manufacturer Country: Germany
Authorized Representative: SMARTECH MEDICAL 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 and plastic surgical devices
Product Type (Level 2): I4800 General Surgery Manual Instrument
Import Information: Imported from abroad

Dates and status

Registration Date: Dec 22, 2016
Expiry Date: Dec 22, 2021

About this record

Access comprehensive regulatory information for "Efinger" Manual surgical instrument for general use (Non-Sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 3404df8cb578c813da3857921cf45995 and manufactured by EFINGER INSTRUMENTS GMBH & CO. KG. The authorized representative in Taiwan is SMARTECH MEDICAL CO., LTD..

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