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cobas MAY - Indonesia BPOM Medical Device Registration

cobas MAY is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20303321170. The device is manufactured by ROCHE MOLECULAR SYSTEM, INC., USA from United States, 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
cobas MAY

cobas MAI

Analysis ID: AKL 20303321170

Risk Classification

Kelas Resiko : B

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

May 30, 2023

Expiry Date

Jan 24, 2028

Product Type

Serological Reagents

Nucleic acid-based in vitro diagnostics devices for the detection of Mycobacterium tuberculosis complex in respiratory specimens (kit & cair)

Invitro Diagnostics

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