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ORANTECH SpO2 Sensor - Indonesia BPOM Medical Device Registration

ORANTECH SpO2 Sensor is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20502122976. The device is manufactured by ORANTECH INC. from China, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. GAMAMED.

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
ORANTECH SpO2 Sensor
Analysis ID: AKL 20502122976

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Manufacturer

ORANTECH INC.

Country of Origin

China

Authorized Representative

PT. GAMAMED

AR Address

JL. WR. SUPRATMAN 56 B

Registration Date

May 21, 2021

Expiry Date

Mar 05, 2026

Product Type

Monitoring Cardiology Equipment

Oximeter.

Non Electromedic Non Sterile

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