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PUREMED Pulse Oximeter - Indonesia BPOM Medical Device Registration

PUREMED Pulse Oximeter is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20502127661. 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 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
PUREMED Pulse Oximeter
Analysis ID: AKL 20502127661

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

China

Authorized Representative

ROYAL SEJAHTERA MANDIRI

AR Address

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

Registration Date

Sep 10, 2024

Expiry Date

Sep 10, 2027

Product Type

Monitoring Cardiology Equipment

Oximeter.

Non Radiation Electromedics

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