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NISSEI Pulse Oximeter - Indonesia BPOM Medical Device Registration

NISSEI Pulse Oximeter is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20502917307. The device is manufactured by NIHON SEIMITSU SOKKI CO.,LTD from Japan, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. MEGA PRATAMA MEDICALINDO.

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
NISSEI Pulse Oximeter
Analysis ID: AKL 20502917307

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

Japan

Authorized Representative

PT. MEGA PRATAMA MEDICALINDO

AR Address

Jl. Pluit Raya 133 Blok A.3

Registration Date

Apr 16, 2024

Expiry Date

Mar 01, 2029

Product Type

Monitoring Cardiology Equipment

Oximeter.

Non Radiation Electromedics

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