DOSI-FUSER Portable Elastomeric Infuser - Indonesia BPOM Medical Device Registration
DOSI-FUSER Portable Elastomeric Infuser is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20902718088. The device is manufactured by LEVENTON, S.A.U. from Spain, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is AMPM HEALTHCARE INDONESIA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
LEVENTON, S.A.U.Country of Origin
Spain
Authorized Representative
AMPM HEALTHCARE INDONESIAAR Address
Jl.Cengkeh Kav.16 No.29-30
Registration Date
Mar 22, 2022
Expiry Date
Nov 01, 2026
Product Type
Therapeutic General and Individual Hospital Equipment
Infusion pump.
Non Electromedic Sterile
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