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RIMSA Examination Lamp - Indonesia BPOM Medical Device Registration

RIMSA Examination Lamp is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 10903510108. The device is manufactured by RIMSA P. LONGONI S.R.L. from Italy, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is PT. CITRA DIAN PRATAMA.

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 : A
RIMSA Examination Lamp
Analysis ID: AKL 10903510108

Risk Classification

Kelas Resiko : A

Product Class

Kelas : 1

Country of Origin

Italy

Authorized Representative

PT. CITRA DIAN PRATAMA

AR Address

Perkantoran Tomang Tol Raya Blok A1 No. 7, Taman Kedoya Baru 11520

Registration Date

Jun 30, 2021

Expiry Date

Sep 10, 2025

Product Type

General Hospital Equipment and Other Individuals

AC-powered medical examination light.

Non Radiation Electromedics

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