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JOULE Multi-Platform Laser/Light System - Indonesia BPOM Medical Device Registration

JOULE Multi-Platform Laser/Light System is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21603324679. The device is manufactured by SCITON, INC. from United States, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is STENIA MEDIKA.

This page provides comprehensive regulatory information including complete registration details, manufacturer information, authorized representative details, product classification, and related products. Pure Global AI offers free access to 67,600+ Indonesia medical device registrations, helping global MedTech companies identify partners, analyze markets, and discover business opportunities efficiently.

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BPOM Registered
Risk Class Kelas Resiko : C
JOULE Multi-Platform Laser/Light System
Analysis ID: AKL 21603324679

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Manufacturer

SCITON, INC.

Country of Origin

United States

Authorized Representative

STENIA MEDIKA

AR Address

GD. Maspion Plaza Lt. 2 Unit I, Jl. Gunung Sahari Raya Kav. 18, Kel. Pademangan Barat, Kec. Pademangan, Kota Adm. Jakarta Utara, Provinsi DKI Jakarta, Kode Pos 14420

Registration Date

Aug 14, 2023

Expiry Date

Mar 13, 2028

Product Type

Surgical Equipment

Laser surgical instrument for use in general and plastic surgery and in dermatology.

Non Radiation Electromedics

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