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COBAS p 471 Centrifuge Unit - Indonesia BPOM Medical Device Registration

COBAS p 471 Centrifuge Unit is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 10209320739. The device is manufactured by ROCHE DIAGNOSTICS AUTOMATION SOLUTIONS GMBH from Germany, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is PT. ROCHE INDONESIA.

This page provides comprehensive regulatory information including complete registration details, manufacturer information, authorized representative details, product classification, and related products. Pure Global AI offers free access to 67,600+ Indonesia medical device registrations, helping global MedTech companies identify partners, analyze markets, and discover business opportunities efficiently.

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BPOM Registered
Risk Class Kelas Resiko : A
COBAS p 471 Centrifuge Unit
Analysis ID: AKL 10209320739

Risk Classification

Kelas Resiko : A

Product Class

Kelas : 1

Country of Origin

Germany

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

Mar 13, 2024

Expiry Date

Sep 26, 2028

Product Type

Products used in the manufacture of blood preparations and preparations of origin and blood

Blood bank centrifuge for in vitro diagnostic use.

Invitro Diagnostics

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