Taiwan FDA registration 67b16248d8838205443c5525e4d910bb

"Geeforis" non-electric coil blade (unsterilized)　

TW: “極福雷斯” 非電力圈刃(未滅菌)　

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

Registration details

Analysis ID: 67b16248d8838205443c5525e4d910bb
Customs Code: DHA04401112001

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 "Geeforis" non-electric coil blade (unsterilized)　 in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 67b16248d8838205443c5525e4d910bb and manufactured by G-FLEX EUROPE SPRL. The authorized representative in Taiwan is KINGDOM EAST ENTERPRISE CO., LTD..

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