Taiwan FDA registration d67235c567a645c5a8983c5e9d767315

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

TW: "巴特克" 一般手術用手動式器械 (未滅菌)

Taiwan·Risk Class 1·MD·BENTEC ENDOSCOPY GMBH·Registered Sep 26, 2019 – Sep 26, 2024Expired

Registration details

Analysis ID: d67235c567a645c5a8983c5e9d767315
License Form: Ministry of Health Medical Device Import No. 020905
Customs Code: DHA09402090505

Company information

Manufacturer: BENTEC ENDOSCOPY GMBH
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: Sep 26, 2019
Expiry Date: Sep 26, 2024

About this record

Access comprehensive regulatory information for "BENTEC" 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 d67235c567a645c5a8983c5e9d767315 and manufactured by BENTEC ENDOSCOPY GMBH. The authorized representative in Taiwan is SMARTECH MEDICAL CO., LTD..

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