OXOID E Coli O157 Latex - Indonesia BPOM Medical Device Registration
OXOID E Coli O157 Latex is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20303818208. The device is manufactured by OXOID LIMITED. from United Kingdom, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. DIPA PUSPA LABSAINS.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
OXOID LIMITED.Country 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
Nov 25, 2022
Expiry Date
Sep 26, 2025
Product Type
Serological Reagents
Escherichia coli serological reagents.
Invitro Diagnostics
OXOID Cary-Blair Medium
OXOID Triple Sugar Iron Agar
OXOID Streptomycin 10 µg
OXOID Doxycycline 30 µg
OXOID Tigecycline 15 µg
OXOID Tobramycin 10 Microgram
OXOID Cefixime 5 µg
OXOID Linezolid 30 µg
OXOID Aztreonam 30 µg
OXOID Azithromycin 15 µg
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