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AIM Malaria Duo Rapid Test (PAN / P. Falciparum) - Indonesia BPOM Medical Device Registration

AIM Malaria Duo Rapid Test (PAN / P. Falciparum) is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20303321007. The device is manufactured by TULIP DIAGNOSTICS (P) LTD. from India, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. ACCURATE INTAN MADYA.

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
AIM Malaria Duo Rapid Test (PAN / P. Falciparum)
Analysis ID: AKL 20303321007

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

India

Authorized Representative

PT. ACCURATE INTAN MADYA

AR Address

KOMPLEK DUTA MERLIN, BLOK. F5 & F6, JL. GAJAH MADA NO. 3-5

Registration Date

Aug 14, 2024

Expiry Date

Aug 14, 2027

Product Type

Serological Reagents

Plasmodium species antigen detection assays

Invitro Diagnostics

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