Taiwan FDA registration 4ed5480cbba6268fddbd8ceb648498c3

"Kanglidu" Hengmei Scar Patch (Unsterilized)

TW: "康力得" 恆美疤痕貼片 (未滅菌)

Taiwan·Risk Class 1·Oriental Innovation Development Co., Ltd. Biomedical Factory·Registered Oct 16, 2015 – Oct 16, 2020Cancelled

Registration details

Analysis ID: 4ed5480cbba6268fddbd8ceb648498c3

Company information

Manufacturer: Oriental Innovation Development Co., Ltd. Biomedical Factory
Manufacturer Country: Taiwan, Province of China
Authorized Representative: CORELEADER BIOTECH CO., LTD.

Product details

Intended Use: Limited to the first-level recognition range of the Measures for the Administration of Medical Devices "Scar Treatment Silicone Products (I.4025)".
Product Type (Level 1): I General, Plastic Surgery and Dermatology
Product Type (Level 2): I.4025 Silicone products for scar treatment
Import Information: 國產;; 委託製造;; QMS/QSD

Dates and status

Registration Date: Oct 16, 2015
Expiry Date: Oct 16, 2020
Cancellation Date: Jun 22, 2022

Cancellation information

Status: Logged out
Reason: 許可證已逾有效期

About this record

Access comprehensive regulatory information for "Kanglidu" Hengmei Scar Patch (Unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 4ed5480cbba6268fddbd8ceb648498c3 and manufactured by Oriental Innovation Development Co., Ltd. Biomedical Factory. The authorized representative in Taiwan is CORELEADER BIOTECH CO., LTD..

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