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LULLABY Resus Plus - Indonesia BPOM Medical Device Registration

LULLABY Resus Plus is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20403512046. The device is manufactured by WIPRO GE HEALTHCARE PVT. LTD. from India, 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
LULLABY Resus Plus
Analysis ID: AKL 20403512046

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Country of Origin

India

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

Feb 23, 2023

Expiry Date

Feb 16, 2026

Product Type

Therapeutic Anesthesia Equipment

Powered emergency ventilator.

Non Electromedic Non Sterile

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