Pure Global

HEISZ Gas Medical Manifold System - Indonesia BPOM Medical Device Registration

HEISZ Gas Medical Manifold System is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 10402126862. The device is manufactured by NANJING OCEAN MEDICAL PRODUCTS CO., LTD. from China, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is PT. HEISZCO ATARA SINDO.

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.

Free Database
Powered by Pure Global AI
BPOM Registered
Risk Class Kelas Resiko : A
HEISZ Gas Medical Manifold System
Analysis ID: AKL 10402126862

Risk Classification

Kelas Resiko : A

Product Class

Kelas : 1

Country of Origin

China

Authorized Representative

PT. HEISZCO ATARA SINDO

AR Address

Komplek Lodan Center Blok D No.7,Jl. Lodan Raya No.2, Rt 01/01, Kel Ancol, Kec Pademangan, Kota Administrasi Jakarta Utara , DKI Jakarta.

Registration Date

Nov 11, 2021

Expiry Date

May 08, 2024

Product Type

Monitoring Anesthesia Equipment

Pressure regulator.

Non Radiation Electromedics

Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing