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TRITON Intensive Care Ventilator - Indonesia BPOM Medical Device Registration

TRITON Intensive Care Ventilator is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20403719487. The device is manufactured by TRITON ELECTRONIC SYSTEMS LTD. from Russian Federation, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. MAIN COMMERCIAL HOSPI.

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 : C
TRITON Intensive Care Ventilator
Analysis ID: AKL 20403719487

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Country of Origin

Russian Federation

Authorized Representative

PT. MAIN COMMERCIAL HOSPI

AR Address

JL. TAMAN MEKAR AGUNG NO. 32-33 RT.003-RW.006 KEL. MEKARWANGI, KEC. BOJONGLOA KIDUL - KOTA BANDUNG

Registration Date

Jun 08, 2022

Expiry Date

May 06, 2024

Product Type

Therapeutic Anesthesia Equipment

Continuous ventilator.

Non Radiation Electromedics

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