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RODENSTOCK Integrated Refraction System - Indonesia BPOM Medical Device Registration

RODENSTOCK Integrated Refraction System is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 11201025583. The device is manufactured by RODENSTOCK INSTRUMENTS BUSINESS UNIT OF TOMEY GMBH. from Germany, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is PT. EAST RAYA LESTARI.

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
RODENSTOCK Integrated Refraction System
Analysis ID: AKL 11201025583

Risk Classification

Kelas Resiko : A

Product Class

Kelas : 1

Country of Origin

Germany

Authorized Representative

PT. EAST RAYA LESTARI

AR Address

Jl. Rawa Kepiting No. 4, Kawasan Industri Pulogadung

Registration Date

Nov 17, 2023

Expiry Date

Jun 20, 2028

Product Type

Diagnostic Eye Equipment

Ophthalmic refractometer.

Non Radiation Electromedics

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