SCHEBO M2-PK™ ELISA Stool Test - Indonesia BPOM Medical Device Registration
SCHEBO M2-PK™ ELISA Stool Test is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20306420236. The device is manufactured by SCHEBO BIOTECH from Germany, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. FRIMUST ADIJAYA UTAMA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
SCHEBO BIOTECHCountry of Origin
Germany
Authorized Representative
PT. FRIMUST ADIJAYA UTAMAAR Address
JL. PEMUDA NO. M3
Registration Date
Nov 15, 2024
Expiry Date
Jul 12, 2029
Product Type
Tumor Antigen Immunologic Test System
Tumor-associated antigen immunological test system.
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