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AMA HELIC Ammonia Breath Test - Indonesia BPOM Medical Device Registration

AMA HELIC Ammonia Breath Test is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20303817593. The device is manufactured by ASSOCIATION OF MEDICINE AND ANALYTICS COMPANY LTD. from Russian Federation, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. MEDQUEST JAYA GLOBAL.

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
AMA HELIC Ammonia Breath Test
Analysis ID: AKL 20303817593

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

Russian Federation

Authorized Representative

PT. MEDQUEST JAYA GLOBAL

AR Address

Menara Salemba Lantai 6 Jl. Salemba Raya Kav. 5 - 5A

Registration Date

Aug 02, 2022

Expiry Date

Jun 07, 2027

Product Type

Serological Reagents

Campylobacter fetus serological reagents.

Invitro Diagnostics

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