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COBAS Deproteinizer - Indonesia BPOM Medical Device Registration

COBAS Deproteinizer is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 10204610840. The device is manufactured by ROCHE DIAGNOSTICS INTERNATIONAL, LTD. from Switzerland, 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 Deproteinizer
Analysis ID: AKL 10204610840

Risk Classification

Kelas Resiko : A

Product Class

Kelas : 1

Country of Origin

Switzerland

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

Dec 23, 2024

Expiry Date

Sep 04, 2029

Product Type

Reagents and Specimen Providers

General purpose reagent.

Invitro Diagnostics

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