EUROIMMUN Anti-Chlamydia Trachomatis ELISA (IgM) - Indonesia BPOM Medical Device Registration

EUROIMMUN Anti-Chlamydia Trachomatis ELISA (IgM) is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20303810029. 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-Chlamydia Trachomatis ELISA (IgM)

Analysis ID: AKL 20303810029

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

Gandaria 8 Office Tower Lantai 16 Unit F Jl. Sultan Iskandar Muda No. 8 RT 010 RW 006

Registration Date

Nov 25, 2024

Expiry Date

Aug 30, 2028

Product Type

Serological Reagents

Chlamydia serological reagents.

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 : C

EUROIMMUN Anti-Chlamydia Trachomatis 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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