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AGAPPE Alkaline Phospatase - Indonesia BPOM Medical Device Registration

AGAPPE Alkaline Phospatase is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20101613082. The device is manufactured by AGAPPE DIAGNOSTIC SWISTERLAND GMBH. from Switzerland, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is 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 Alkaline Phospatase
Analysis ID: AKL 20101613082

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

Switzerland

Authorized Representative

MULTIMEDILAB KARYAMANDIRI

AR Address

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

Registration Date

Mar 16, 2022

Expiry Date

Dec 15, 2025

Product Type

Clinical Chemistry Test System

Alkaline phosphatase or isoenzymes test system (kit & cair)

Invitro Diagnostics

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