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CITEST ™ FSH Test Cassette (Whole Blood/Serum/Plasma) - Indonesia BPOM Medical Device Registration

CITEST ™ FSH Test Cassette (Whole Blood/Serum/Plasma) is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20101420382. The device is manufactured by CITEST DIAGNOSTICS INC from Canada, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. NELTA MULTI GRACIA.

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BPOM Registered
Risk Class Kelas Resiko : B
CITEST ™ FSH Test Cassette (Whole Blood/Serum/Plasma)
Analysis ID: AKL 20101420382

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

Canada

Authorized Representative

PT. NELTA MULTI GRACIA

AR Address

Metland Menteng. Jl. Menteng Niaga Blok J7 No.1 Ujung Menteng, Cakung, Jakarta Timur 13960

Registration Date

Mar 08, 2024

Expiry Date

Feb 20, 2026

Product Type

Clinical Chemistry Test System

Follicle-stimulating hormone test system (card)

Invitro Diagnostics

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