EUROIMMUN Anti - CCP ELISA (IgG) - Indonesia BPOM Medical Device Registration

EUROIMMUN Anti - CCP ELISA (IgG) is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20305610435. 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.

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

EUROIMMUN Anti - CCP ELISA (IgG)

Analysis ID: AKL 20305610435

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

Jul 29, 2024

Expiry Date

Aug 30, 2028

Product Type

Immunological Test System

Rheumatoid factor immunological test system.

Invitro Diagnostics

DJ Fang

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Other Products from EUROIMMUN MEDIZINISCHE LABORDIAGNOSTIKA AG.

Products from the same manufacturer (10 products)

EUROIMMUN MEDIZINISCHE LABORDIAGNOSTIKA AG

Kelas Resiko : B

EUROIMMUN Anti - CCP ELISA (IgG) - 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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