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EASYRA Albumin Reagent Kit (ALB) - Indonesia BPOM Medical Device Registration

EASYRA Albumin Reagent Kit (ALB) is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20101511023. The device is manufactured by MEDICA CORPORATION. from United States, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is SABA INDOMEDIKA.

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 : B
EASYRA Albumin Reagent Kit (ALB)
Analysis ID: AKL 20101511023

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

United States

Authorized Representative

SABA INDOMEDIKA

AR Address

Ruko Kedoya Elok Plaza DB-33 Jl. Panjang No.7-9

Registration Date

Oct 05, 2023

Expiry Date

May 03, 2028

Product Type

Clinical Chemistry Test System

Albumin test system (kit & cair)

Invitro Diagnostics

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