Taiwan FDA registration 3ae343d02335268c5b5055b4da04b315

"Weiji" manual instrument for general surgery (unsterilized)

TW: "威堤" 一般手術用手動式器械 (未滅菌)

Taiwan·Risk Class 1·WITTE GMBH·Registered Apr 21, 2006 – Apr 21, 2021Cancelled

Registration details

Analysis ID: 3ae343d02335268c5b5055b4da04b315
Customs Code: DHA04400412609

Company information

Manufacturer: WITTE GMBH
Manufacturer Country: Germany
Authorized Representative: WONDERFUL INSTRUMENTS COMPANY, 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, Plastic Surgery and Dermatology
Product Type (Level 2): I.4800 Hand Instruments for General Surgery
Import Information: import

Dates and status

Registration Date: Apr 21, 2006
Expiry Date: Apr 21, 2021
Cancellation Date: Oct 12, 2023

Cancellation information

Status: Logged out
Reason: 未展延而逾期者

About this record

Access comprehensive regulatory information for "Weiji" manual instrument for general surgery (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 3ae343d02335268c5b5055b4da04b315 and manufactured by WITTE GMBH. The authorized representative in Taiwan is WONDERFUL INSTRUMENTS COMPANY, LTD..

This page provides complete technical specifications, regulatory compliance details. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.