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AGAPPE Microalbumin MISPA i3 - Indonesia BPOM Medical Device Registration

AGAPPE Microalbumin MISPA i3 is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20305124978. The device is manufactured by AGAPPE DIAGNOSTICS LTD. from India, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. MULTIMEDILAB KARYAMANDIRI.

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
AGAPPE Microalbumin MISPA i3
Analysis ID: AKL 20305124978

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

India

Authorized Representative

PT. MULTIMEDILAB KARYAMANDIRI

AR Address

GP plaza lantai 3 unit 6, jalan Gelora II No. 01

Registration Date

Aug 12, 2021

Expiry Date

Dec 16, 2025

Product Type

Immunological Test System

Albumin immunological test system.

Invitro Diagnostics

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