Dimension Phosphorus Flex (PHOS) reagent cartridge - Indonesia BPOM Medical Device Registration

Dimension Phosphorus Flex (PHOS) reagent cartridge is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20101220868. The device is manufactured by SIEMENS HEALTHCARE DIAGNOSTICS INC. from United States, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is SIEMENS HEALTHINEERS INDONESIA.

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BPOM Registered

Risk Class Kelas Resiko : B

Dimension Phosphorus Flex (PHOS) reagent cartridge

Analysis ID: AKL 20101220868

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Manufacturer

SIEMENS HEALTHCARE DIAGNOSTICS INC.

Country of Origin

United States

Authorized Representative

SIEMENS HEALTHINEERS INDONESIA

AR Address

Perkantoran Hijau Arkadia Tower F, Lantai 18, Jl.Tahi Bonar Simatupang Kav. 88

Registration Date

Feb 06, 2025

Expiry Date

Aug 01, 2029

Product Type

Clinical Chemistry Test System

Phosphorus (inorganic) test system (kit & cair)

Invitro Diagnostics

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Dimension Phosphorus Flex (PHOS) reagent cartridge - 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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