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

CITEST ™ D-Dimer Test Cassette (Whole Blood/Plasma) is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20207420177. The device is manufactured by CITEST DIAGNOSTICS INC from Canada, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. NELTA MULTI GRACIA.

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BPOM Registered

Risk Class Kelas Resiko : C

CITEST ™ D-Dimer Test Cassette (Whole Blood/Plasma)

Analysis ID: AKL 20207420177

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Manufacturer

CITEST DIAGNOSTICS INC

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

Nov 01, 2024

Expiry Date

Feb 20, 2026

Product Type

Haematology Package and Kit

Fibrinogen/fibrin degradation products assay.

Invitro Diagnostics

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

Risk Classification

Product Class

Manufacturer

Country of Origin

Authorized Representative

AR Address

Registration Date

Expiry Date

Product Type

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