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BECKMAN COULTER CD11c-PE - Indonesia BPOM Medical Device Registration

BECKMAN COULTER CD11c-PE is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 10201320701. The device is manufactured by IMMUNOTECH S.A.S., A BECKMAN COULTER COMPANY from France, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is PT. FOCUS DIAGNOSTIC INDONESIA.

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Risk Class Kelas Resiko : A
BECKMAN COULTER CD11c-PE
Analysis ID: AKL 10201320701

Risk Classification

Kelas Resiko : A

Product Class

Kelas : 1

Country of Origin

France

Authorized Representative

PT. FOCUS DIAGNOSTIC INDONESIA

AR Address

Jl. Jatipadang Raya No.9A, RT.6/RW.4, Kelurahan Jatipadang, Kecamatan Pasar Minggu, Kota Jakarta Selatan, DKI Jakarta 12540

Registration Date

Dec 26, 2024

Expiry Date

Dec 31, 2027

Product Type

Biological Dyes

Immunohistochemistry reagents and kits (Qualitative).

Invitro Diagnostics

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