STREPTAVIDIN-PE - Indonesia BPOM Medical Device Registration
STREPTAVIDIN-PE is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20304420117. The device is manufactured by IMMUCOR GTI DIAGNOSTICS, INC. from United States, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. BIOMED GLOBAL SINERGI.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
IMMUCOR GTI DIAGNOSTICS, INC.Country of Origin
United States
Authorized Representative
PT. BIOMED GLOBAL SINERGIAR Address
JL. GAJAH MADA No.156 B LANTAI 1
Registration Date
Dec 16, 2024
Expiry Date
Jun 17, 2029
Product Type
Immunology Laboratory Equipment and Reagents
Complement reagent.
Invitro Diagnostics
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LIFECODES HLA-A eRES SSO TYPING KIT For Use with Luminex
LIFECODES HLA-DRB 3, 4, 5 SSO Typing Kit For Use With Luminex
LIFECODES HLA-B eRES SSO TYPING KIT For Use with Luminex
LIFECODES HLA-DPA1/B1 SSO Typing Kit For Use With Luminex
LIFECODES HLA-C eRES SSO TYPING KIT For Use with Luminex
LIFECODES LSA ™ Class II
COFOE Blood Glucose Meter
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LIFECODES LifeScreen Deluxe
IMMUCOR GTI DIAGNOSTICS, INC.
LIFECODES HLA-DRB1 eRES SSO TYPING KIT For Use with Luminex
IMMUCOR GTI DIAGNOSTICS, INC.
LIFECODES HLA-A eRES SSO TYPING KIT For Use with Luminex
IMMUCOR GTI DIAGNOSTICS, INC.
LIFECODES HLA-DPA1/B1 SSO Typing Kit For Use With Luminex
IMMUCOR GTI DIAGNOSTICS, INC.
LIFECODES HLA-B eRES SSO TYPING KIT For Use with Luminex
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