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MISONIX Sonastar Ultrasonic Surgical Asporation System - Indonesia BPOM Medical Device Registration

MISONIX Sonastar Ultrasonic Surgical Asporation System is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21603420411. The device is manufactured by MISONIX INC. from United States, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. SIGMA KARSA MAGNA.

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BPOM Registered
Risk Class Kelas Resiko : B
MISONIX Sonastar Ultrasonic Surgical Asporation System
Analysis ID: AKL 21603420411

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Manufacturer

MISONIX INC.

Country of Origin

United States

Authorized Representative

PT. SIGMA KARSA MAGNA

AR Address

Ruko Mega Grosir Cempaka Mas, Jl. Letjen Suprapto Blok J No. 37-38 RW.08, Kel. Sumur Batu, Kota Adm. Jakarta Pusat, Provinsi DKI Jakarta

Registration Date

Feb 19, 2024

Expiry Date

Sep 12, 2027

Product Type

Surgical Equipment

Ultrasonic surgical instrument

Non Radiation Electromedics

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