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GENTEC OxyBlend Air/Oxygen Blender - Indonesia BPOM Medical Device Registration

GENTEC OxyBlend Air/Oxygen Blender is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20403812966. The device is manufactured by GENTEC (SHANGHAI) CORPORATION. from China, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. MEDISTRON ENERGY.

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
GENTEC OxyBlend Air/Oxygen Blender
Analysis ID: AKL 20403812966

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

China

Authorized Representative

PT. MEDISTRON ENERGY

AR Address

Ruko Cinere Terrace Commercial Blok JC No. 5, Jl. Telaga Warna

Registration Date

Oct 09, 2019

Expiry Date

Dec 31, 2023

Product Type

Therapeutic Anesthesia Equipment

Breathing gas mixer.

Non Electromedic Non Sterile

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