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GE AISYS CS2 - Indonesia BPOM Medical Device Registration

GE AISYS CS2 is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20403410478. The device is manufactured by DATEX- OHMEDA INC., from United States, 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.

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BPOM Registered
Risk Class Kelas Resiko : C
GE AISYS CS2
Analysis ID: AKL 20403410478

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

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

Jun 21, 2022

Expiry Date

Jun 11, 2025

Product Type

Therapeutic Anesthesia Equipment

Gas machine for anesthesia or analgesia.

Non Radiation Electromedics

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