GRIFOLS Anti-Jka for DG Gel - Indonesia BPOM Medical Device Registration
GRIFOLS Anti-Jka for DG Gel is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20209420216. The device is manufactured by MEDION GRIFOLS DIAGNOSTICS AG from Switzerland, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. FRISMED HOSLAB INDONESIA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
MEDION GRIFOLS DIAGNOSTICS AGCountry of Origin
Switzerland
Authorized Representative
PT. FRISMED HOSLAB INDONESIAAR Address
Ruko Bidex Blok G No. 30-31 Jl. Pahlawan Seribu BSD City, 15321
Registration Date
Feb 05, 2025
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.
Invitro Diagnostics
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