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COBAS 8000 C 502 Module and Accessories - Indonesia BPOM Medical Device Registration

COBAS 8000 C 502 Module and Accessories is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20102515774. The device is manufactured by HITACHI HIGH TECHNOLOGIES CORP. from Japan, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. ROCHE INDONESIA.

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BPOM Registered
Risk Class Kelas Resiko : B
COBAS 8000 C 502 Module and Accessories
Analysis ID: AKL 20102515774

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

Japan

Authorized Representative

PT. ROCHE INDONESIA

AR Address

Gedung AIA Central Lantai 36 Jl. Jend. Sudirman KAV. 48A RT/RW 003/004 Kelurahan Karet Semanggi

Registration Date

Jul 29, 2019

Expiry Date

Feb 12, 2024

Product Type

Clinical Laboratory Equipment

Instrumentation for clinical multiplex test systems.

Invitro Diagnostics

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