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FUTURA SYSTEM Creatinine 4+1 - Indonesia BPOM Medical Device Registration

FUTURA SYSTEM Creatinine 4+1 is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20101918091. The device is manufactured by FUTURA SYSTEM GROUP S.R.L. from Italy, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. PRIORITA DIAN SARANA.

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BPOM Registered
Risk Class Kelas Resiko : B
FUTURA SYSTEM Creatinine 4+1
Analysis ID: AKL 20101918091

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

Italy

Authorized Representative

PT. PRIORITA DIAN SARANA

AR Address

Jl. RSI. Faisal Raya No. 06

Registration Date

Apr 25, 2024

Expiry Date

May 30, 2028

Product Type

Clinical Chemistry Test System

Creatinine test system (kit & cair)

Invitro Diagnostics

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