Taiwan FDA registration 04977a73df5219a81edebc3bea7c2484

"Visharp" non-powered urological surgical instruments and their accessories (unsterilized)

TW: “威夏普”非動力式泌尿科手術器械及其附件 (未滅菌)

Taiwan·Risk Class 1·WISAP MEDICAL TECHNOLOGY GMBH·Registered Jun 15, 2006 – Jun 15, 2021Cancelled

Registration details

Analysis ID: 04977a73df5219a81edebc3bea7c2484
Customs Code: DHA04400470805

Company information

Manufacturer: WISAP MEDICAL TECHNOLOGY GMBH
Manufacturer Country: Germany
Authorized Representative: BEAMED INSTRUMENTS CO., LTD.

Product details

Intended Use: Limited to the first level identification scope of the Measures for the Administration of Medical Devices "Manual Gastroenterology-Urology Surgical Instruments and Their Accessories (H.4730)".
Product Type (Level 1): H Gastroenterology and urology
Product Type (Level 2): H.4730 H.4730 Hand Gastroentero-Urology Surgical Instruments and Accessories
Import Information: import

Dates and status

Registration Date: Jun 15, 2006
Expiry Date: Jun 15, 2021
Cancellation Date: Aug 28, 2023

Cancellation information

Status: Logged out
Reason: 許可證已逾有效期

About this record

Access comprehensive regulatory information for "Visharp" non-powered urological surgical instruments and their accessories (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 04977a73df5219a81edebc3bea7c2484 and manufactured by WISAP MEDICAL TECHNOLOGY GMBH. The authorized representative in Taiwan is BEAMED INSTRUMENTS CO., LTD..

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