OXOID Dnase Agar - Indonesia BPOM Medical Device Registration
OXOID Dnase Agar is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 10302813828. The device is manufactured by OXOID LIMITED from United Kingdom, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is PT. DIPA PUSPA LABSAINS.
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Risk Classification
Product Class
Kelas : 1
Manufacturer
OXOID LIMITEDCountry of Origin
United Kingdom
Authorized Representative
PT. DIPA PUSPA LABSAINSAR Address
Dipa Strategic Office, Lantai Lobby, Jl. Raya Kebayoran Lama No.28 RT.009/RW.011, Kel. Grogol Utara, Kec. Kebayoran Lama
Registration Date
Dec 29, 2022
Expiry Date
Sep 26, 2025
Product Type
Microbiology Equipment
Selective culture medium.
Invitro Diagnostics
OXOID Bacitracin 10 IU
OXOID Urea Agar Base
OXOID Alkaline Peptone Water
BRILLIANCE Salmonella Agar Base
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OXOID Eosin Methylene Blue Agar (Levine)
OXOID Brain Heart Infusion Broth
OXOID Neomycin 30 Microgram
OXOID Ofloxacin 5 µg
OXOID Teicoplanin TEC 30 µg
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