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ONCOPROBE Rapid Drug Panel 7 in 1 (AMP/MOR/THC/BZD/METH/COC/SOMA - Indonesia BPOM Medical Device Registration

ONCOPROBE Rapid Drug Panel 7 in 1 (AMP/MOR/THC/BZD/METH/COC/SOMA is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20103023767. The device is manufactured by CAL-TECH DIAGNOSTIC INC. from United States, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. MAIN ONCOPROBE.

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BPOM Registered
Risk Class Kelas Resiko : C
ONCOPROBE Rapid Drug Panel 7 in 1 (AMP/MOR/THC/BZD/METH/COC/SOMA
Analysis ID: AKL 20103023767

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Country of Origin

United States

Authorized Representative

PT. MAIN ONCOPROBE

AR Address

APRT.ISTANA HARMONI LT.DASAR UNIT 1M, KOMP.HARMONI PLAZA JL.SURYOPRANOTO NO.2, PETOJO UTARA

Registration Date

Jul 16, 2023

Expiry Date

Jul 14, 2026

Product Type

Clinical Toxicology Test System

Multi parameter clinical toxicology test system

Invitro Diagnostics

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Kelas Resiko : C

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Kelas Resiko : B

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Kelas Resiko : B

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Kelas Resiko : B

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Kelas Resiko : C