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FOCUS Syphicheck WB device - Indonesia BPOM Medical Device Registration

FOCUS Syphicheck WB device is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20303220397. The device is manufactured by ZEPHYR BIOMEDICALS - A DIV. OF TULIP DIAGNOSTICS (P) LTD. from India, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. FOCUS DIAGNOSTIC INDONESIA.

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BPOM Registered
Risk Class Kelas Resiko : C
FOCUS Syphicheck WB device

FOKUS Syphicheck WB device

Analysis ID: AKL 20303220397

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Country of Origin

India

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

Jan 24, 2025

Expiry Date

Jan 23, 2028

Product Type

Serological Reagents

Treponema pallidum treponemal test reagents.

Invitro Diagnostics

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