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PUREMED Medical Oxygen Regulator - Indonesia BPOM Medical Device Registration

PUREMED Medical Oxygen Regulator is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 10402912338. 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. 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 : A
PUREMED Medical Oxygen Regulator
Analysis ID: AKL 10402912338

Risk Classification

Kelas Resiko : A

Product Class

Kelas : 1

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 17, 2023

Expiry Date

Nov 15, 2026

Product Type

Monitoring Anesthesia Equipment

Pressure regulator.

Non Electromedic Sterile

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