Taiwan FDA registration 420e2e23c9dc0b7e2d182653dfa9b74f

"Medis" diode laser treatment instrument and its accessories

TW: “麥迪斯”二極體雷射治療儀及其配件

Taiwan·Risk Class 2·SURGICAL LASER TECHNOLOGIES, A DIVISION OF PHOTOMEDEX, INC.·Registered Nov 14, 2008 – Nov 14, 2013Cancelled

Registration details

Analysis ID: 420e2e23c9dc0b7e2d182653dfa9b74f
Customs Code: DHA00601934901

Company information

Manufacturer: SURGICAL LASER TECHNOLOGIES, A DIVISION OF PHOTOMEDEX, INC.
Manufacturer Country: United States
Authorized Representative: LITE-MED 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: import

Dates and status

Registration Date: Nov 14, 2008
Expiry Date: Nov 14, 2013
Cancellation Date: May 28, 2015

Cancellation information

Status: Logged out
Reason: 許可證已逾有效期

About this record

Access comprehensive regulatory information for "Medis" diode laser treatment instrument and its accessories in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 420e2e23c9dc0b7e2d182653dfa9b74f and manufactured by SURGICAL LASER TECHNOLOGIES, A DIVISION OF PHOTOMEDEX, INC.. The authorized representative in Taiwan is LITE-MED INC..

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