Taiwan FDA registration 61efd1e9a4bc9b45ce3293c54a703f84

"Geforres" Manual Gastroenterological Instruments and Their Accessories (Unsterilized)

TW: "極福雷斯" 手動式胃腸科手術器械及其附件 (未滅菌)

Taiwan·Risk Class 1·G-FLEX EUROPE SPRL·Registered Nov 30, 2011 – Nov 30, 2021Cancelled

Registration details

Analysis ID: 61efd1e9a4bc9b45ce3293c54a703f84
Customs Code: DHA04401111903

Company information

Manufacturer: G-FLEX EUROPE SPRL
Manufacturer Country: Belgium
Authorized Representative: KINGDOM EAST ENTERPRISE 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: Nov 30, 2011
Expiry Date: Nov 30, 2021
Cancellation Date: Sep 19, 2023

Cancellation information

Status: Logged out
Reason: 自行鍵入

About this record

Access comprehensive regulatory information for "Geforres" Manual Gastroenterological 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 61efd1e9a4bc9b45ce3293c54a703f84 and manufactured by G-FLEX EUROPE SPRL. The authorized representative in Taiwan is KINGDOM EAST ENTERPRISE CO., 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.