EUROIMMUN Anti-Rubella Virus Glycoprotein ELISA (IgM) - Indonesia BPOM Medical Device Registration

EUROIMMUN Anti-Rubella Virus Glycoprotein ELISA (IgM) is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20303021065. The device is manufactured by EUROIMMUN MEDIZINISCHE LABORDIAGNOSTIKA AG. from Germany, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is INTI MAKMUR MEDITAMA.

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BPOM Registered

Risk Class Kelas Resiko : C

EUROIMMUN Anti-Rubella Virus Glycoprotein ELISA (IgM)

Analysis ID: AKL 20303021065

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Manufacturer

EUROIMMUN MEDIZINISCHE LABORDIAGNOSTIKA AG.

Country of Origin

Germany

Authorized Representative

INTI MAKMUR MEDITAMA

AR Address

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

Registration Date

Aug 19, 2024

Expiry Date

Aug 30, 2028

Product Type

Serological Reagents

Rubella virus serological reagents.

Invitro Diagnostics

DJ Fang

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EUROIMMUN MEDIZINISCHE LABORDIAGNOSTIKA AG.

Kelas Resiko : C

EUROIMMUN Anti-Rubella Virus Glycoprotein ELISA (IgM) - 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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