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APMA HealthCare Infusion Pump HK-100II - Indonesia BPOM Medical Device Registration

APMA HealthCare Infusion Pump HK-100II is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20902121295. The device is manufactured by SHENZHEN HAWK MEDICAL INSTRUMENT CO., LTD. from China, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. ANUGERAH PUTRA MANDIRI ALKESINDO.

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
APMA HealthCare Infusion Pump HK-100II
Analysis ID: AKL 20902121295

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

China

Authorized Representative

PT. ANUGERAH PUTRA MANDIRI ALKESINDO

AR Address

JL. RATU AYU II NO.10 WAGE-TAMAN.SIDOARJO

Registration Date

Mar 13, 2021

Expiry Date

Mar 09, 2024

Product Type

Therapeutic General and Individual Hospital Equipment

Infusion pump.

Non Radiation Electromedics

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