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GE Giraffe Blue Spot PT Lite - Indonesia BPOM Medical Device Registration

GE Giraffe Blue Spot PT Lite is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20902413026. The device is manufactured by LUMITEX INC. from United States, 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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BPOM Registered
Risk Class Kelas Resiko : B
GE Giraffe Blue Spot PT Lite
Analysis ID: AKL 20902413026

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Manufacturer

LUMITEX INC.

Country of Origin

United States

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

Sep 07, 2023

Expiry Date

Dec 29, 2027

Product Type

Therapeutic General and Individual Hospital Equipment

Infant radiant warmer.

Non Radiation Electromedics

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