HUMAN SLE LATEX TEST - Indonesia BPOM Medical Device Registration
HUMAN SLE LATEX TEST is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20305120284. The device is manufactured by HUMAN GESELLSCHAFT FÜR BIOCHEMICA UND DIAGNOSTICA MBH from Germany, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. SALI POLAPA TOGETHER.
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Risk Classification
Product Class
Kelas : 2
Country of Origin
Germany
Authorized Representative
PT. SALI POLAPA TOGETHERAR Address
Puri Sentra Niaga Blok B 33-34 Jl. Raya Kalimalang 13620
Registration Date
Oct 07, 2024
Expiry Date
Nov 08, 2027
Product Type
Immunological Test System
Systemic lupus erythematosus immunological test system.
Invitro Diagnostics
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HUMAN Transferrin
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HUMAN Calcium Liquicolor HumaStar
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