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RODENSTOCK Auto Refractometer - Indonesia BPOM Medical Device Registration

RODENSTOCK Auto Refractometer is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 11201917788. The device is manufactured by SHANGHAI SUPORE INSTRUMENTS CO., LTD. from China, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is PT. ALFA INTERNAL OPTINDO.

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 Auto Refractometer
Analysis ID: AKL 11201917788

Risk Classification

Kelas Resiko : A

Product Class

Kelas : 1

Country of Origin

China

Authorized Representative

PT. ALFA INTERNAL OPTINDO

AR Address

JALAN KAREL SATSUIT TUBUN NOMOR 72 LANTAI 1 RT.001 / RW.001

Registration Date

May 15, 2024

Expiry Date

Jan 01, 2029

Product Type

Diagnostic Eye Equipment

Ophthalmic refractometer.

Non Radiation Electromedics

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