MINDRAY BeneHeart C2 Fully Automatic (Automated External Defibrillator(AED)) - Indonesia BPOM Medical Device Registration

MINDRAY BeneHeart C2 Fully Automatic (Automated External Defibrillator(AED)) is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 30505918764. The device is manufactured by SHENZHEN MINDRAY BIO-MEDICAL ELECTRONICS CO.,LTD from China, and is classified as Risk Class Kelas Resiko : D. The authorized representative in Indonesia is PT. MINDRAY MEDICAL INDONESIA.

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BPOM Registered

Risk Class Kelas Resiko : D

MINDRAY BeneHeart C2 Fully Automatic (Automated External Defibrillator(AED))

Analysis ID: AKL 30505918764

Risk Classification

Kelas Resiko : D

Product Class

Kelas : 3

Manufacturer

SHENZHEN MINDRAY BIO-MEDICAL ELECTRONICS CO.,LTD

Country of Origin

China

Authorized Representative

PT. MINDRAY MEDICAL INDONESIA

AR Address

Menara DEA II Lt.17, Jl. Mega Kuningan Barat Kav.E4.3 No.1-2, Kel. Kuningan Timur, Kec.Setiabudi Kawasan Mega Kuningan, Jakarta Selatan

Registration Date

Aug 02, 2024

Expiry Date

Apr 09, 2029

Product Type

Therapeutic Cardiology Equipment

Automated external defibrillator.

Non Radiation Electromedics

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MINDRAY BeneHeart C2 Fully Automatic (Automated External Defibrillator(AED)) - Indonesia BPOM Medical Device Registration

Risk Classification

Product Class

Manufacturer

Country of Origin

Authorized Representative

AR Address

Registration Date

Expiry Date

Product Type

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