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NESCO O2 Medical Oxygen Regulator - Indonesia BPOM Medical Device Registration

NESCO O2 Medical Oxygen Regulator is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 10402612495. The device is manufactured by YUYAO JIAHUA MEDICAL APPLIANCE CO., LTD. from China, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is PT. DJUNIAR & DJUNIAR.

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 : A
NESCO O2 Medical Oxygen Regulator
Analysis ID: AKL 10402612495

Risk Classification

Kelas Resiko : A

Product Class

Kelas : 1

Country of Origin

China

Authorized Representative

PT. DJUNIAR & DJUNIAR

AR Address

KOMPLEK RUKAN MAHKOTA ANCOL BLOK D NO. 26

Registration Date

Nov 11, 2020

Expiry Date

Nov 11, 2023

Product Type

Monitoring Anesthesia Equipment

Pressure regulator.

Non Electromedic Non Sterile

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