Diomni™ Software v4.0 - Indonesia BPOM Medical Device Registration
Diomni™ Software v4.0 is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20102320717. The device is manufactured by LIFE TECHNOLOGIES HOLDINGS PTE. LTD. from Singapore, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is MURSMEDIC.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
LIFE TECHNOLOGIES HOLDINGS PTE. LTD.Country of Origin
Singapore
Authorized Representative
MURSMEDICAR Address
The Kensington Office Tower Lantai 11, Jalan Boulevard Raya Nomor 1, Desa/Kelurahan Kelapa Gading Timur, Kec. Kelapa Gading, Kota Adm. Jakarta Utara, Provinsi DKI Jakarta, 14240
Registration Date
Nov 29, 2023
Expiry Date
Aug 29, 2028
Product Type
Clinical Laboratory Equipment
Instrumentation for clinical multiplex test systems.
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