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MEDICA EO Hemoconcentrator - Indonesia BPOM Medical Device Registration

MEDICA EO Hemoconcentrator is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20805220226. The device is manufactured by MEDICA S.P.A. from Italy, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. TERUMO INDONESIA.

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
MEDICA EO Hemoconcentrator
Analysis ID: AKL 20805220226

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Manufacturer

MEDICA S.P.A.

Country of Origin

Italy

Authorized Representative

PT. TERUMO INDONESIA

AR Address

Wisma Keiai Lt.5 Jl. Jend.Sudirman Kav.3 Jakarta

Registration Date

Oct 29, 2024

Expiry Date

Feb 28, 2027

Product Type

Therapeutic Gastroenterology-Urology Equipment

High permeability hemodialysis system.

Non Electromedic Sterile

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