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TOSOH ST AIA-PACK PAP - Indonesia BPOM Medical Device Registration

TOSOH ST AIA-PACK PAP is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20101710010. The device is manufactured by TOSOH AIA INC. from Japan, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. KARINDO ALKESTRON.

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BPOM Registered
Risk Class Kelas Resiko : B
TOSOH ST AIA-PACK PAP
Analysis ID: AKL 20101710010

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Manufacturer

TOSOH AIA INC.

Country of Origin

Japan

Authorized Representative

PT. KARINDO ALKESTRON

AR Address

JL. TOMANG RAYA NO.17

Registration Date

Jul 17, 2020

Expiry Date

Nov 20, 2024

Product Type

Clinical Chemistry Test System

Acid phosphatase (total or prostatic) test system (kit & cair)

Invitro Diagnostics

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