DG CellMedia - Indonesia BPOM Medical Device Registration
DG CellMedia is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20209220181. The device is manufactured by DIAGNOSTIC GRIFOLS, S.A from Spain, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is FRISMED HOSLAB INDONESIA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
DIAGNOSTIC GRIFOLS, S.ACountry of Origin
Spain
Authorized Representative
FRISMED HOSLAB INDONESIAAR Address
Ruko Bidex Blok G No. 30-31 Jl. Pahlawan Seribu BSD City, 15321
Registration Date
Nov 28, 2023
Expiry Date
Mar 01, 2026
Product Type
Products used in the manufacture of blood preparations and preparations of origin and blood
Automated blood grouping and antibody test system.
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