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Cl- Electrode COBAS INTEGRA ISE Modules - Indonesia BPOM Medical Device Registration

Cl- Electrode COBAS INTEGRA ISE Modules is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20101614949. The device is manufactured by ROCHE DIAGNOSTICS INTL, LTD. from Switzerland, and is classified as Risk Class Kelas Resiko : B. 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 : B
Cl- Electrode COBAS INTEGRA ISE Modules
Analysis ID: AKL 20101614949

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

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

Apr 05, 2023

Expiry Date

Jan 26, 2026

Product Type

Clinical Chemistry Test System

Chloride test system (card)

Invitro Diagnostics

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