CODAN Syringe Pump - Indonesia BPOM Medical Device Registration
CODAN Syringe Pump is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20902815316. The device is manufactured by CODAN ARGUS AG. from Switzerland, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. DEMKA SAKTI.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
CODAN ARGUS AG.Country of Origin
Switzerland
Authorized Representative
PT. DEMKA SAKTIAR Address
Jl. Tanah Abang III No. 19 A - B, Jakarta Pusat
Registration Date
Dec 12, 2022
Expiry Date
Jun 29, 2026
Product Type
Therapeutic General and Individual Hospital Equipment
Infusion pump.
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