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MagNA Pure 24 Instrument and Accessories - Indonesia BPOM Medical Device Registration

MagNA Pure 24 Instrument and Accessories is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20304220099. The device is manufactured by ROCHE DIAGNOSTICS INTERNATIONAL LTD. from Switzerland, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is ROCHE INDONESIA.

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BPOM Registered
Risk Class Kelas Resiko : C
MagNA Pure 24 Instrument and Accessories
Analysis ID: AKL 20304220099

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Country of Origin

Switzerland

Authorized Representative

ROCHE INDONESIA

AR Address

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

Registration Date

Sep 29, 2022

Expiry Date

Mar 03, 2027

Product Type

Immunology Laboratory Equipment and Reagents

RNA Preanalytical Systems.

Invitro Diagnostics

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