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TREVIOLUX Photodynamic Therapy Devices - Indonesia BPOM Medical Device Registration

TREVIOLUX Photodynamic Therapy Devices is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21603420900. The device is manufactured by MEDLIGHT, GMBH from Germany, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. AESENDIA INFINI INDONESIA.

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BPOM Registered
Risk Class Kelas Resiko : B
TREVIOLUX Photodynamic Therapy Devices
Analysis ID: AKL 21603420900

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Manufacturer

MEDLIGHT, GMBH

Country of Origin

Germany

Authorized Representative

PT. AESENDIA INFINI INDONESIA

AR Address

Business Park Kebon Jeruk Blok D2 No. 10, Jl. Meruya Ilir Raya No. 88, Kode Pos 11620

Registration Date

Apr 24, 2024

Expiry Date

Oct 19, 2025

Product Type

Surgical Equipment

Ultraviolet lamp for dermatologic disorders.

Non Radiation Electromedics

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