HILL-ROM® 900 Accella ™ Bed - Indonesia BPOM Medical Device Registration
HILL-ROM® 900 Accella ™ Bed is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20902918935. The device is manufactured by HILL-ROM S.A.S from France, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is IDS MEDICAL SYSTEMS INDONESIA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
HILL-ROM S.A.SCountry of Origin
France
Authorized Representative
IDS MEDICAL SYSTEMS INDONESIAAR Address
Gedung Wisma 76, Lantai 17 & 22, Jl. LetJend. S. Parman Kav.76, Kelurahan Slipi, Kecamatan Palmerah, 11410
Registration Date
Sep 11, 2024
Expiry Date
Dec 31, 2026
Product Type
Therapeutic General and Individual Hospital Equipment
AC-powered adjustable hospital bed.
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