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SONOSCAPE Light Source - Indonesia BPOM Medical Device Registration

SONOSCAPE Light Source is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20801022541. The device is manufactured by SONOSCAPE MEDICAL CORPORATION. from China, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is ENDO INDONESIA.

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 : B
SONOSCAPE Light Source
Analysis ID: AKL 20801022541

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

China

Authorized Representative

ENDO INDONESIA

AR Address

Jl. Raya Menganti 14

Registration Date

Oct 04, 2023

Expiry Date

Dec 31, 2026

Product Type

Diagnostic Gastroenterology-Urology Equipment

Endoscope and accessories

Non Radiation Electromedics

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