Taiwan FDA registration c4b304b9bc15eb7f41d3b1ba0095a003

"Tekno" MANUAL SURGICAL INSTRUMENT BOX (Non-Sterile)

TW: "泰克諾" 器械盒 (未滅菌)

Taiwan·Risk Class 1·MD·TEKNO-MEDICAL OPTIK-CHIRURGIE GMBH.·Registered Jul 03, 2017 – Jul 03, 2022Expired

Registration details

Analysis ID: c4b304b9bc15eb7f41d3b1ba0095a003
License Form: Ministry of Health Medical Device Import No. 018033
Customs Code: DHA09401803308

Company information

Manufacturer: TEKNO-MEDICAL OPTIK-CHIRURGIE GMBH.
Manufacturer Country: Germany
Authorized Representative: T-SUN 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 and plastic surgical devices
Product Type (Level 2): I4800 General Surgery Manual Instrument
Import Information: Imported from abroad

Dates and status

Registration Date: Jul 03, 2017
Expiry Date: Jul 03, 2022

About this record

Access comprehensive regulatory information for "Tekno" MANUAL SURGICAL INSTRUMENT BOX (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 c4b304b9bc15eb7f41d3b1ba0095a003 and manufactured by TEKNO-MEDICAL OPTIK-CHIRURGIE GMBH.. The authorized representative in Taiwan is T-SUN INTERNATIONAL CO., LTD..

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