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cobas CT/NG - Indonesia BPOM Medical Device Registration

cobas CT/NG is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20303321014. The device is manufactured by ROCHE MOLECULAR SYSTEM, INC., USA from United States, and is classified as Risk Class Kelas Resiko : C. 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 : C
cobas CT/NG
Analysis ID: AKL 20303321014

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Country of Origin

United States

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 06, 2023

Expiry Date

Aug 31, 2027

Product Type

Serological Reagents

Multiparameter serological reagents

Invitro Diagnostics

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