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RIMED Digi-Lite - Indonesia BPOM Medical Device Registration

RIMED Digi-Lite is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21501220520. The device is manufactured by RIMED LTD from Israel, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is INTERGASTRA archipelago.

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
RIMED Digi-Lite
Analysis ID: AKL 21501220520

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Manufacturer

RIMED LTD

Country of Origin

Israel

Authorized Representative

INTERGASTRA archipelago

AR Address

Pangeran Jayakarta 24/34-35 Mangga Dua Selatan Sawah Besar- Jakarta Pusat

Registration Date

Oct 27, 2022

Expiry Date

Dec 31, 2025

Product Type

Diagnostic Radiology Equipment

Ultrasonic pulsed doppler imaging system.

Non Radiation Electromedics

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