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AMS 200FA - Indonesia BPOM Medical Device Registration

AMS 200FA is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20102420008. The device is manufactured by URIT MEDICAL ELECTRONIC CO.,LTD from China, 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 200FA
Analysis ID: AKL 20102420008

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

China

Authorized Representative

PT. TIRTA PASIFIK MEDIKATAMA

AR Address

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

Registration Date

Jan 05, 2024

Expiry Date

Jan 04, 2027

Product Type

Clinical Laboratory Equipment

Clinical chemistry analyzer

Invitro Diagnostics

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