VITRO Cervico-Vaginal Self Collection Kit - Indonesia BPOM Medical Device Registration
VITRO Cervico-Vaginal Self Collection Kit is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 10302220217. The device is manufactured by VITRO S.A. from Spain, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is PT. GRAHA MEGATAMA INDONESIA.
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Risk Classification
Product Class
Kelas : 1
Manufacturer
VITRO S.A.Country of Origin
Spain
Authorized Representative
PT. GRAHA MEGATAMA INDONESIAAR Address
RUKO MAHKOTA ANCOL BLOK. E 39 JL. BUDI MULIA KEL. PADEMANGAN BARAT
Registration Date
Dec 09, 2022
Expiry Date
Aug 04, 2027
Product Type
Microbiology Equipment
Microbiological specimen collection and transport device.
Invitro Diagnostics
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VITRO Bacterial CNS Flow Chip Kit (Hybridization Reagents)
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VITRO hybriSpot24
VITRO S.A.
VITRO Flow Chip Hybridization Reagents Type I (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 hybriSpot12
VITRO S.A.
VITRO Sepsis Flow Chip Kit (Hybridiation Reagents)
VITRO S.A.
VITRO HybriSpot 12 PCR Auto
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.