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"Kinty" in vivo with unabsorbed gauze (sterilized/unsterilized) - Taiwan Registration fe97a4b2af42786b6053e0a2e93fc9ad

Access comprehensive regulatory information for "Kinty" in vivo with unabsorbed gauze (sterilized/unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number fe97a4b2af42786b6053e0a2e93fc9ad and manufactured by HENAN KELONG MEDICAL APPARATUS AND INSTRUMENTS CO., LTD.. The authorized representative in Taiwan is KING DAY CO., LTD..

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fe97a4b2af42786b6053e0a2e93fc9ad
Registration Details
Taiwan FDA Registration: fe97a4b2af42786b6053e0a2e93fc9ad
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Device Details

"Kinty" in vivo with unabsorbed gauze (sterilized/unsterilized)
TW: "้‡‘่’‚"้ซ”ๅ…ง็”จไธ่ขซๅธๆ”ถ็ด—ๅธƒ(ๆป…่Œ/ๆœชๆป…่Œ)
Risk Class 1
Cancelled

Registration Details

fe97a4b2af42786b6053e0a2e93fc9ad

DHA04600190202

Company Information

Product Details

Limited to the first level of identification range of "unabsorbed gauze for in vivo (I.4450)" under the Measures for the Administration of Medical Devices.

I General, Plastic Surgery and Dermatology

I.4450 Non-absorbable filament cloth for internal use

QMS/QSD;; Chinese goods;; input

Dates and Status

May 31, 2013

May 31, 2018

Nov 20, 2019

Cancellation Information

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