VITRO Sepsis Flow Chip Kit (Hybridiation Reagents) - Indonesia BPOM Medical Device Registration
VITRO Sepsis Flow Chip Kit (Hybridiation Reagents) is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20303122785. The device is manufactured by VITRO S.A. from Spain, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. GRAHA MEGATAMA INDONESIA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
VITRO S.A.Country of Origin
Spain
Authorized Representative
PT. GRAHA MEGATAMA INDONESIAAR Address
BIZ PARK 3 COMMERCIAL ESTATE BLOK E NOMOR 9, JALAN SULTAN AGUNG KM 28.5
Registration Date
Feb 05, 2025
Expiry Date
Apr 28, 2027
Product Type
Serological Reagents
Nucleic acid-based device for the amplification, detection, and identification of microbial pathogens directly from whole blood specimens.
Invitro Diagnostics
VITRO hybriSpot24
VITRO HybriSpot 12 PCR Auto
VITRO hybriSpot12
VITRO Sepsis Flow Chip Kit (PCR Reagents)
VITRO Bacterial CNS Flow Chip Kit (Hybridization Reagents)
VITRO Bacterial CNS Flow Chip Kit (PCR Reagents)
VITRO STD Direct Flow Chip Kit (PCR Reagents)
VITRO HPV Direct Flow Chip Kit (PCR Reagents)
VITRO Respiratory Flow Chip Kit (PCR Reagents)
VITRO Cervico-Vaginal Self Collection Kit
VITRO Flow Chip Hybridization Reagents Type I (Auto)
VITRO S.A
VITRO hybriSpot24
VITRO S.A.
VITRO hybriSpot12
VITRO S.A.
VITRO HybriSpot 12 PCR Auto
VITRO S.A.
VITRO Sepsis Flow Chip Kit (PCR Reagents)
VITRO S.A.
VITRO Bacterial CNS Flow Chip Kit (Hybridization Reagents)
VITRO S.A.
VITRO Bacterial CNS Flow Chip Kit (PCR Reagents)
VITRO S.A.
VITRO HPV Direct Flow Chip Kit (Hybridization Reagents)
VITRO S.A
VITRO STD Direct Flow Chip Kit (PCR Reagents)
VITRO S.A.
VITRO HPV Direct Flow Chip Kit (PCR Reagents)
VITRO S.A.