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MPM Silicone Manual Resuscitator Set - Indonesia BPOM Medical Device Registration

MPM Silicone Manual Resuscitator Set is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20403420287. The device is manufactured by BESMED HEALTH BUSINESS CORP from Taiwan (China), and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. MEGA PRATAMA MEDICALINDO.

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BPOM Registered
Risk Class Kelas Resiko : B
MPM Silicone Manual Resuscitator Set
Analysis ID: AKL 20403420287

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

Taiwan (China)

Authorized Representative

PT. MEGA PRATAMA MEDICALINDO

AR Address

Jl. Pluit Raya 133 Blok A.3

Registration Date

Apr 05, 2024

Expiry Date

Dec 19, 2026

Product Type

Therapeutic Anesthesia Equipment

Manual emergency ventilator.

Non Electromedic Non Sterile

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