HOSPITECH Heart Lung Pack II - Indonesia BPOM Medical Device Registration

HOSPITECH Heart Lung Pack II is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20504220032. The device is manufactured by HOSPITECH MANUFACTURING SERVICES SDN. BHD. from Malaysia, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. GEM OF MOTHER ARTANO.

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

HOSPITECH Heart Lung Pack II

Analysis ID: AKL 20504220032

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Manufacturer

HOSPITECH MANUFACTURING SERVICES SDN. BHD.

Country of Origin

Malaysia

Authorized Representative

PT. GEM OF MOTHER ARTANO

AR Address

Jl. Hos. Cokroaminoto, Komp. Perkantoran CBD Ciledug Blok A3 No. 17, Ciledug 15157

Registration Date

Apr 13, 2022

Expiry Date

Feb 01, 2026

Product Type

Surgical Cardiology Equipment

Cardiopulmonary bypass vascular catheter, cannula, or tubing.

Non Electromedic Sterile

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