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Brivo NM 615 - Indonesia BPOM Medical Device Registration

Brivo NM 615 is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21501412107. The device is manufactured by GE HUALUN MEDICAL SYSTEM CO., LTD., CHINA. from China, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. GE OPERATIONS INDONESIA.

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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Risk Class Kelas Resiko : B
Brivo NM 615
Analysis ID: AKL 21501412107

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

China

Authorized Representative

PT. GE OPERATIONS INDONESIA

AR Address

South Quarter Tower B, Lantai 18-19 Jl. R.A. Kartini, Kav. 8 Kel. Cilandak Barat, Kec. Cilandak Jakarta Selataran 12430

Registration Date

Mar 11, 2019

Expiry Date

Dec 13, 2023

Product Type

Diagnostic Radiology Equipment

Scintillation (gamma) camera.

Non Radiation Electromedics

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