Taiwan FDA registration 623c40e55b8a98554006094de50b720c

"/ S Arthur" in vitro cosmetic repair supplement (unsterilized)

TW: "/眽S亞瑟克" 體外美容用修復彌補物 (未滅菌)

Taiwan·Risk Class 1·ZELTIQ AESTHETICS, INC.·Registered Dec 30, 2010 – Dec 30, 2015Cancelled

Registration details

Analysis ID: 623c40e55b8a98554006094de50b720c
Customs Code: DHA04400976108

Company information

Manufacturer: ZELTIQ AESTHETICS, INC.
Manufacturer Country: United States
Authorized Representative: Conservation Corporation Limited

Product details

Intended Use: Limited to the first level recognition range of medical equipment management measures for in vitro cosmetic repair supplements (I.3800).
Product Type (Level 1): I General, Plastic Surgery and Dermatology
Product Type (Level 2): I.3800 Repair supplement for cosmetic use in the body
Import Information: import

Dates and status

Registration Date: Dec 30, 2010
Expiry Date: Dec 30, 2015
Cancellation Date: Jun 25, 2018

Cancellation information

Status: Logged out
Reason: 許可證已逾有效期

About this record

Access comprehensive regulatory information for "/ S Arthur" in vitro cosmetic repair supplement (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 623c40e55b8a98554006094de50b720c and manufactured by ZELTIQ AESTHETICS, INC.. The authorized representative in Taiwan is Conservation Corporation Limited.

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