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µALB Calibrator Kit - Indonesia BPOM Medical Device Registration

µALB Calibrator Kit is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20101124681. 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 PT. 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
µALB Calibrator Kit
Analysis ID: AKL 20101124681

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Manufacturer

MEDICA CORPORATION

Country of Origin

United States

Authorized Representative

PT. SABA INDOMEDIKA

AR Address

KOMP.KEDOYA ELOK PLAZA KAV DB/33 KEDOYA SELATAN

Registration Date

Nov 06, 2021

Expiry Date

Dec 31, 2023

Product Type

Clinical Chemistry Test System

Calibrator (cair)

Invitro Diagnostics

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