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"Geeforis" non-electric coil blade (unsterilized)  - Taiwan Registration 67b16248d8838205443c5525e4d910bb

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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67b16248d8838205443c5525e4d910bb
Registration Details
Taiwan FDA Registration: 67b16248d8838205443c5525e4d910bb
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Device Details

"Geeforis" non-electric coil blade (unsterilized) 
TW: “極福雷斯” 非電力圈刃(未滅菌) 
Risk Class 1
Cancelled

Registration Details

67b16248d8838205443c5525e4d910bb

DHA04401112001

Company Information

Belgium

Product Details

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)".

H Gastroenterology and urology

H.4730 H.4730 Hand Gastroentero-Urology Surgical Instruments and Accessories

import

Dates and Status

Nov 30, 2011

Nov 30, 2021

Sep 19, 2023

Cancellation Information

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