Taiwan FDA registration fe97a4b2af42786b6053e0a2e93fc9ad

"Kinty" in vivo with unabsorbed gauze (sterilized/unsterilized)

TW: "金蒂"體內用不被吸收紗布(滅菌/未滅菌)

Taiwan·Risk Class 1·HENAN KELONG MEDICAL APPARATUS AND INSTRUMENTS CO., LTD.·Registered May 31, 2013 – May 31, 2018Cancelled

Registration details

Analysis ID: fe97a4b2af42786b6053e0a2e93fc9ad
Customs Code: DHA04600190202

Company information

Manufacturer: HENAN KELONG MEDICAL APPARATUS AND INSTRUMENTS CO., LTD.
Manufacturer Country: China
Authorized Representative: KING DAY CO., LTD.

Product details

Intended Use: 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.
Product Type (Level 1): I General, Plastic Surgery and Dermatology
Product Type (Level 2): I.4450 Non-absorbable filament cloth for internal use
Import Information: QMS/QSD;; Chinese goods;; input

Dates and status

Registration Date: May 31, 2013
Expiry Date: May 31, 2018
Cancellation Date: Nov 20, 2019

Cancellation information

Status: Logged out
Reason: 許可證已逾有效期

About this record

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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