Taiwan FDA registration 96233c119a50366c403855da78525395

"Illipus" shuttle laser hand grip

TW: “伊利普斯”飛梭雷射手握把

Taiwan·Risk Class 2·ELLIPSE A/S·Registered Feb 22, 2017 – Feb 22, 2022Cancelled

Registration details

Analysis ID: 96233c119a50366c403855da78525395
Customs Code: DHA05602946301

Company information

Manufacturer: ELLIPSE A/S
Manufacturer Country: Denmark
Authorized Representative: DYNAMIC MEDICAL TECHNOLOGIES INC.

Product details

Intended Use: For details, it is Chinese approved copy of the imitation order
Product Type (Level 1): I General, Plastic Surgery and Dermatology
Product Type (Level 2): I.4810 Lasers for general surgical, orthopaedic and dermatological use
Import Information: Input;; The use of this device shall comply with the provisions of the Administrative Measures for the Implementation or Use of Medical Devices for Specific Medical Technology Inspection and Testing.

Dates and status

Registration Date: Feb 22, 2017
Expiry Date: Feb 22, 2022
Cancellation Date: Apr 12, 2024

Cancellation information

Status: Logged out
Reason: 許可證已逾有效期

About this record

Access comprehensive regulatory information for "Illipus" shuttle laser hand grip in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 96233c119a50366c403855da78525395 and manufactured by ELLIPSE A/S. The authorized representative in Taiwan is DYNAMIC MEDICAL TECHNOLOGIES INC..

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