Taiwan FDA registration 9cf6db68cea5610258947330b89d878d

〝H&H〞Scar Care Sheet (Non-Sterile)

TW: 〝H&H〞疤痕貼片 (未滅菌)

Taiwan·Risk Class 1·MD·TRONJEN MEDICAL TECHNOLOGY INC.·Registered Aug 02, 2021 – Aug 02, 2026Active

Registration details

Analysis ID: 9cf6db68cea5610258947330b89d878d
License Form: Ministry of Health Medical Device Manufacturing No. 009209

Company information

Manufacturer: TRONJEN MEDICAL TECHNOLOGY INC.
Manufacturer Country: Taiwan, Province of China
Authorized Representative: TRONJEN MEDICAL TECHNOLOGY INC.

Product details

Intended Use: Limited to the first level identification scope of the Measures for the Classification and Grading of Medical Devices "Scar Treatment Silicone Products (I.4025)".
Product Type (Level 1): I General and plastic surgical devices
Product Type (Level 2): I4025 Scar Treatment Silicone Products
Import Information: Produced in Taiwan, China

Dates and status

Registration Date: Aug 02, 2021
Expiry Date: Aug 02, 2026

About this record

Access comprehensive regulatory information for 〝H&H〞Scar Care Sheet (Non-Sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 9cf6db68cea5610258947330b89d878d and manufactured by TRONJEN MEDICAL TECHNOLOGY INC.. The authorized representative in Taiwan is TRONJEN MEDICAL TECHNOLOGY INC..

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