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NOVALISA Dengue Virus IgM - Indonesia BPOM Medical Device Registration

NOVALISA Dengue Virus IgM is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20303818286. The device is manufactured by NOVATEC IMMUNODIAGNOSTICA GMBH from Germany, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is BESTARI SUKSES MAKMUR.

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 : C
NOVALISA Dengue Virus IgM
Analysis ID: AKL 20303818286

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Country of Origin

Germany

Authorized Representative

BESTARI SUKSES MAKMUR

AR Address

Kokan Permata Kelapa Gading Blok E No. 5 Jl. Boulevard Bukit Gading Raya, Kel. Gading Barat, Kec. Kelapa Gading, Jakarta Utara

Registration Date

May 30, 2022

Expiry Date

Aug 31, 2024

Product Type

Serological Reagents

Dengue virus serological reagents

Invitro Diagnostics

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