EUROLINE Inhalation South East Asia (IgE) - Indonesia BPOM Medical Device Registration

EUROLINE Inhalation South East Asia (IgE) is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20305025065. The device is manufactured by EUROIMMUN MEDIZINISCHE LABORDIAGNOSTIKA AG. from Germany, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. INTI MAKMUR MEDITAMA.

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BPOM Registered

Risk Class Kelas Resiko : B

EUROLINE Inhalation South East Asia (IgE)

Analysis ID: AKL 20305025065

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Manufacturer

EUROIMMUN MEDIZINISCHE LABORDIAGNOSTIKA AG.

Country of Origin

Germany

Authorized Representative

PT. INTI MAKMUR MEDITAMA

AR Address

JL. SULTAN ISKANDAR MUDA, GANDARIA 8 OFFICE TOWER LANTAI 16 UNIT F, KEBAYORAN LAMA JAKARTA SELATAN

Registration Date

Mar 08, 2022

Expiry Date

Dec 31, 2024

Product Type

Immunological Test System

Immunoglobulins A, G, M, D, and E immunological test system.

Invitro Diagnostics

DJ Fang

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EUROLINE Inhalation South East Asia (IgE) - Indonesia BPOM Medical Device Registration

Risk Classification

Product Class

Manufacturer

Country of Origin

Authorized Representative

AR Address

Registration Date

Expiry Date

Product Type

DJ Fang

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