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GREATCARE Manual Resuscitator - Indonesia BPOM Medical Device Registration

GREATCARE Manual Resuscitator is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20403127493. The device is manufactured by NINGBO GREATCARE TRADING CO.,LTD from China, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is LUMARY BIRUMAS.

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
GREATCARE Manual Resuscitator
Analysis ID: AKL 20403127493

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

China

Authorized Representative

LUMARY BIRUMAS

AR Address

Gd. Menara Palma Lt. 12 Jl. H.R. Rasuna Said Blok X-2, Kav.6 Jakarta 12950

Registration Date

May 14, 2024

Expiry Date

Apr 19, 2029

Product Type

Therapeutic Anesthesia Equipment

Manual emergency ventilator.

Non Electromedic Non Sterile

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DJ Fang

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