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BE CARE Pulse Oximeter - Indonesia BPOM Medical Device Registration

BE CARE Pulse Oximeter is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20502320910. The device is manufactured by SHENZHEN IMDK MEDICAL TECHNOLOGY CO, LTD from China, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. ROYAL SEJAHTERA MANDIRI.

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
BE CARE Pulse Oximeter
Analysis ID: AKL 20502320910

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

China

Authorized Representative

PT. ROYAL SEJAHTERA MANDIRI

AR Address

Ruko Mahkota Ancol Blok E No.53, Jl. RE Martadinata, Kelurahan Pademanagn Barat

Registration Date

Nov 24, 2023

Expiry Date

Nov 23, 2026

Product Type

Monitoring Cardiology Equipment

Oximeter.

Non Radiation Electromedics

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