Taiwan FDA registration 14d9f5cf542b7a203625235f6b50f837

"Tekno" Manual gastroenterology-urology surgical instrument and accessories (Non-Sterile)

TW: "鈦科諾" 手動式胃腸科-泌尿科手術器械及其附件 (未滅菌)

Taiwan·Risk Class 1·MD·TEKNO-MEDICAL OPTIK-CHIRURGIE GMBH.·Registered Jul 21, 2016 – Jul 21, 2021Cancelled

Registration details

Analysis ID: 14d9f5cf542b7a203625235f6b50f837
License Form: Ministry of Health Medical Device Import No. 016797
Customs Code: DHA09401679700

Company information

Manufacturer: TEKNO-MEDICAL OPTIK-CHIRURGIE GMBH.
Manufacturer Country: Germany
Authorized Representative: MEDEN INTERNATIONAL INC.

Product details

Product Type (Level 1): H Gastroenterology-urology devices
Product Type (Level 2): H4730 Manual gastroenterology-urological surgical instruments and accessories
Import Information: Imported from abroad

Dates and status

Registration Date: Jul 21, 2016
Expiry Date: Jul 21, 2021
Cancellation Date: Aug 09, 2023

Cancellation information

Status: Logged out
Reason: 許可證已逾有效期

About this record

Access comprehensive regulatory information for "Tekno" Manual gastroenterology-urology surgical instrument and accessories (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 14d9f5cf542b7a203625235f6b50f837 and manufactured by TEKNO-MEDICAL OPTIK-CHIRURGIE GMBH.. The authorized representative in Taiwan is MEDEN INTERNATIONAL INC..

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