Taiwan FDA registration 4c2faf2d5a7bc7fc45decded105e9f19

"Baorou" Baorou

TW: "保柔緹" 保柔

Taiwan·Risk Class 3·ANTEIS SA;; Anteis S.A.·Registered Mar 15, 2011 – Mar 15, 2021Cancelled

Registration details

Analysis ID: 4c2faf2d5a7bc7fc45decded105e9f19
Customs Code: DHA00602221901

Company information

Manufacturer: ANTEIS SA;; Anteis S.A.
Manufacturer Country: Switzerland
Authorized Representative: MERZ ASIA PACIFIC PTE. LTD. TAIWAN BRANCH (SINGAPORE)

Product details

Intended Use: This product is an injected implant to increase the volume of skin tissue, which can: 1. Correct the sunken face caused by injury and age; 2. Face contouring such as cheeks, chin, etc.; 3. Lip augmentation (the red edge of the lip increases the three-dimensional curvature; 4. Treatment of medium and deep nasolabial folds.
Product Type (Level 1): I General, Plastic Surgery and Dermatology
Import Information: import

Dates and status

Registration Date: Mar 15, 2011
Expiry Date: Mar 15, 2021
Cancellation Date: Jan 07, 2020

Cancellation information

Status: Logged out
Reason: 自請註銷

About this record

Access comprehensive regulatory information for "Baorou" Baorou in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number 4c2faf2d5a7bc7fc45decded105e9f19 and manufactured by ANTEIS SA;; Anteis S.A.. The authorized representative in Taiwan is MERZ ASIA PACIFIC PTE. LTD. TAIWAN BRANCH (SINGAPORE).

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