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DERMATIX Ultra Advanced Silicone Gel Scar Reduction - Indonesia BPOM Medical Device Registration

DERMATIX Ultra Advanced Silicone Gel Scar Reduction is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21603904079. The device is manufactured by HANSON MEDICAL INC. from United States, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. TRANSFARMA MEDICA INDAH.

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BPOM Registered
Risk Class Kelas Resiko : B
DERMATIX Ultra Advanced Silicone Gel Scar Reduction
Analysis ID: AKL 21603904079

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

United States

Authorized Representative

PT. TRANSFARMA MEDICA INDAH

AR Address

Unit 802, 8th Fl., Wisma Pondok Indah 2 JL. Sultan Iskandar Muda Kav V - TA, Pondok Indah.

Registration Date

Feb 22, 2021

Expiry Date

Jan 26, 2026

Product Type

Surgical Equipment

Hydrogel wound dressing and burn dressing.

Non Electromedic Non Sterile

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