Taiwan FDA registration a8b29cd877213d42326e7b997e8d7bd0

"TEKNO" Manual surgical instruments for general use (Non-Sterile)

TW: "德科隆" 一般手術用手動式器械 (未滅菌)

Taiwan·Risk Class 1·MD·TEKNO MEDICAL OPTIK-CHIRURGIE GMBH·Registered Sep 17, 2019 – Sep 17, 2024Expired

Registration details

Analysis ID: a8b29cd877213d42326e7b997e8d7bd0
License Form: Ministry of Health Medical Device Import No. 020869
Customs Code: DHA09402086901

Company information

Manufacturer: TEKNO MEDICAL OPTIK-CHIRURGIE GMBH
Manufacturer Country: Germany
Authorized Representative: MEDITEK LIFESCIENCES CORP.

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 17, 2019
Expiry Date: Sep 17, 2024

About this record

Access comprehensive regulatory information for "TEKNO" Manual surgical instruments 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 a8b29cd877213d42326e7b997e8d7bd0 and manufactured by TEKNO MEDICAL OPTIK-CHIRURGIE GMBH. The authorized representative in Taiwan is MEDITEK LIFESCIENCES CORP..

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