MIURA 200 Single ARM and Accessories - Indonesia BPOM Medical Device Registration

MIURA 200 Single ARM and Accessories is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20102412260. The device is manufactured by I.S.E. S.R.L. from Italy, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is CAKRA MEDIKA UTAMA.

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BPOM Registered

Risk Class Kelas Resiko : B

MIURA 200 Single ARM and Accessories

Analysis ID: AKL 20102412260

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Manufacturer

Country of Origin

Italy

Authorized Representative

CAKRA MEDIKA UTAMA

AR Address

FORESTA BUSINESS LOFT 6 No. 10, Jl. Raya Boulevard Utara BSD City, Desa/Kelurahan Lengkong Kulon

Registration Date

Jul 16, 2023

Expiry Date

May 31, 2026

Product Type

Clinical Laboratory Equipment

Instrumentation for clinical multiplex test systems.

Invitro Diagnostics

DJ Fang

MedTech Regulatory Expert

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