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PROWESS Panther Treatment Planning System - Indonesia BPOM Medical Device Registration

PROWESS Panther Treatment Planning System is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21501320939. The device is manufactured by PROWESS INC from United States, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. MEDIUM FIRST.

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BPOM Registered
Risk Class Kelas Resiko : B
PROWESS Panther Treatment Planning System
Analysis ID: AKL 21501320939

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Manufacturer

PROWESS INC

Country of Origin

United States

Authorized Representative

PT. MEDIUM FIRST

AR Address

The Bellezza Permata Hijau GP Office Tower Lantai 27 No. 03, Jl. Letjen Soepeno No. 34, Jakarta

Registration Date

May 11, 2023

Expiry Date

Mar 23, 2025

Product Type

Diagnostic Radiology Equipment

Medical image management and processing system.

Non Radiation Electromedics

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