VITRO Flow Chip Hybridization Reagents Type I (Auto) - Indonesia BPOM Medical Device Registration
VITRO Flow Chip Hybridization Reagents Type I (Auto) is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20303025507. 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.ACountry 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 07, 2025
Expiry Date
Apr 28, 2027
Product Type
Serological Reagents
Multiparameter serological reagents
Invitro Diagnostics
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