Pure Global

Lunar iDXA - Indonesia BPOM Medical Device Registration

Lunar iDXA is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21501916221. The device is manufactured by GE MEDICAL SYSTEMS MONTERREY MEXICO S.A. DE C.V. from Mexico, and is classified as Risk Class Kelas Resiko : C. 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.

Free Database
Powered by Pure Global AI
BPOM Registered
Risk Class Kelas Resiko : C
Lunar iDXA
Analysis ID: AKL 21501916221

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Country of Origin

Mexico

Authorized Representative

PT. GE OPERATIONS INDONESIA

AR Address

South Quarter Tower B, Lt. 18-19, Jl. R.A. Kartini Kav. 8

Registration Date

May 03, 2024

Expiry Date

Jan 24, 2029

Product Type

Diagnostic Radiology Equipment

Bone densitometer.

Electromedic Radiation

Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing
Similar Products (1)
Other products with the same name
Other Products from GE MEDICAL SYSTEMS MONTERREY MEXICO S.A. DE C.V.
Products from the same manufacturer (1 products)