Taiwan FDA registration a923a9f1c1805e1b89ed4d04b4e9c85b

"Sgio" nasal and face-enriching implants

TW: “史吉歐”鼻而丰顏面植入物

Taiwan·Risk Class 2·Surgical Technology Laboratories, Inc.·Registered Oct 12, 2017 – Oct 12, 2027Active

Registration details

Analysis ID: a923a9f1c1805e1b89ed4d04b4e9c85b
Customs Code: DHA05603034202

Company information

Manufacturer: Surgical Technology Laboratories, Inc.
Manufacturer Country: United States
Authorized Representative: J-TRUE MEDICAL INTERNATIONAL CO., LTD.

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.3500 Polytetrafluoroethylene (PTFE) implant material containing carbonaceous composites
Import Information: 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". input

Dates and status

Registration Date: Oct 12, 2017
Expiry Date: Oct 12, 2027

About this record

Access comprehensive regulatory information for "Sgio" nasal and face-enriching implants in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number a923a9f1c1805e1b89ed4d04b4e9c85b and manufactured by Surgical Technology Laboratories, Inc.. The authorized representative in Taiwan is J-TRUE MEDICAL INTERNATIONAL CO., LTD..

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