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AMS UREA - Indonesia BPOM Medical Device Registration

AMS UREA is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20101322880. The device is manufactured by SCIENTIFIC MEDICAL PRODUCTS PAZ.SAN.VE TฤฐC. LTD.. STI. from Turkey, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. TIRTA PASIFIK MEDIKATAMA.

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
AMS UREA
Analysis ID: AKL 20101322880

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

Turkey

Authorized Representative

PT. TIRTA PASIFIK MEDIKATAMA

AR Address

JL. Jatibening Raya II, Ruko Jatibening No. 2 RT/RW 03/01

Registration Date

Apr 03, 2023

Expiry Date

Apr 02, 2026

Product Type

Clinical Chemistry Test System

Urea nitrogen test system (kit & cair)

Invitro Diagnostics

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