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EXIAS e|1 Cartridge 150 oQC - Indonesia BPOM Medical Device Registration

EXIAS e|1 Cartridge 150 oQC is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20101022568. The device is manufactured by EXIAS MEDICAL GMBH from Austria, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is EN. RIOCA MEDICA.

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BPOM Registered
Risk Class Kelas Resiko : C
EXIAS e|1 Cartridge 150 oQC
Analysis ID: AKL 20101022568

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Manufacturer

EXIAS MEDICAL GMBH

Country of Origin

Austria

Authorized Representative

EN. RIOCA MEDICA

AR Address

Komplek Pesona Indah Kapuk Blok A6 Jl. Kapuk Kamal Raya Kav.20A Lantai 3

Registration Date

Jan 27, 2024

Expiry Date

Nov 21, 2028

Product Type

Clinical Chemistry Test System

Multi parameter clinical chemistry test system

Invitro Diagnostics

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