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CODAN ARGUS Syringe Pump - Indonesia BPOM Medical Device Registration

CODAN ARGUS Syringe Pump is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20902902959. The device is manufactured by CODAN ARGUS from Switzerland, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. DEMKA SAKTI.

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BPOM Registered
Risk Class Kelas Resiko : B
CODAN ARGUS Syringe Pump
Analysis ID: AKL 20902902959

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Manufacturer

CODAN ARGUS

Country of Origin

Switzerland

Authorized Representative

PT. DEMKA SAKTI

AR Address

Jl. Tanah Abang III No. 19 A - B, Jakarta Pusat

Registration Date

Aug 10, 2021

Expiry Date

Jun 29, 2025

Product Type

Therapeutic General and Individual Hospital Equipment

Infusion pump.

Non Radiation Electromedics

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