CADD-Solis 2110 Ambulatory Infusion Pump - Indonesia BPOM Medical Device Registration
CADD-Solis 2110 Ambulatory Infusion Pump is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20902614702. The device is manufactured by SMITHS MEDICAL ASD INC. from United States, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. IDS MEDICAL SYSTEMS INDONESIA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
SMITHS MEDICAL ASD INC.Country of Origin
United States
Authorized Representative
PT. IDS MEDICAL SYSTEMS INDONESIAAR Address
Gedung Wisma 76, Lantai 17 & 22, Jl. LetJend. S. Parman Kav.76, Kelurahan Slipi, Kecamatan Palmerah, 11410
Registration Date
Dec 23, 2022
Expiry Date
Mar 16, 2025
Product Type
Therapeutic General and Individual Hospital Equipment
Infusion pump.
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