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R-Evolution - Indonesia BPOM Medical Device Registration

R-Evolution is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21203611137. The device is manufactured by OPTIKON 2000 S.P.A. from Italy, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. OPMIC PERKASA MANDIRI.

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 : C
R-Evolution
Analysis ID: AKL 21203611137

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Country of Origin

Italy

Authorized Representative

PT. OPMIC PERKASA MANDIRI

AR Address

Jl.Puri Kencana Blok K7-3D 3rd Fl Kembangan Jakarta 11610

Registration Date

Sep 27, 2024

Expiry Date

Jun 14, 2029

Product Type

Surgical Eye Equipment

Phacofragmentation system.

Non Radiation Electromedics

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