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COBAS 6000 e 601 and Accessories - Indonesia BPOM Medical Device Registration

COBAS 6000 e 601 and Accessories is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20102711139. The device is manufactured by HITACHI HIGH-TECHNOLOGIES CORPORATION. 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 6000 e 601 and Accessories
Analysis ID: AKL 20102711139

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

Jun 17, 2021

Expiry Date

Apr 29, 2026

Product Type

Clinical Laboratory Equipment

Instrumentation for clinical multiplex test systems.

Invitro Diagnostics

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DJ Fang

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