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ACARE Handheld Pulse Oximeter - Indonesia BPOM Medical Device Registration

ACARE Handheld Pulse Oximeter is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20502420161. The device is manufactured by ACARE TECHNOLOGY CO.,LTD. from Taiwan (China), and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is INMED TEKNOTAMA CEMERLANG.

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
ACARE Handheld Pulse Oximeter
Analysis ID: AKL 20502420161

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

Taiwan (China)

Authorized Representative

INMED TEKNOTAMA CEMERLANG

AR Address

Rukan Inkopau Ujung Menteng Blok B No. 31, Il. Sultan Hamengkubuwono IX Km. 25, Kel. Ujung Menteng Kec. Cakung

Registration Date

Apr 29, 2024

Expiry Date

Dec 14, 2028

Product Type

Monitoring Cardiology Equipment

Oximeter.

Non Radiation Electromedics

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