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HOSMED Frey4.3is Syringe Pump - Indonesia BPOM Medical Device Registration

HOSMED Frey4.3is Syringe Pump is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20902125172. The device is manufactured by HOSMED INC. from United States, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. SALSABIL RESA PRADANA.

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BPOM Registered
Risk Class Kelas Resiko : B
HOSMED Frey4.3is Syringe Pump
Analysis ID: AKL 20902125172

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Manufacturer

HOSMED INC.

Country of Origin

United States

Authorized Representative

PT. SALSABIL RESA PRADANA

AR Address

Sentral Senayan II Office Tower Lt.16 Unit 216A Jl. Asia Afrika No.6 Jakarta Pusat

Registration Date

Aug 25, 2021

Expiry Date

Apr 16, 2024

Product Type

Therapeutic General and Individual Hospital Equipment

Infusion pump.

Non Radiation Electromedics

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