DENSICHECK Plus Instrument for VITEK 2 System and Accessories - Indonesia BPOM Medical Device Registration
DENSICHECK Plus Instrument for VITEK 2 System and Accessories is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20301313809. The device is manufactured by BIOMERIEUX INC. from United States, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. ENSEVAL MEDIKA PRIMA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
BIOMERIEUX INC.Country of Origin
United States
Authorized Representative
PT. ENSEVAL MEDIKA PRIMAAR Address
JL. PULO LENTUT NO.12, LT.1 UNIT 1C & LT.2 UNIT 2A, KAWASAN INDUSTRI PULOGADUNG
Registration Date
Jan 06, 2025
Expiry Date
Dec 31, 2028
Product Type
Diagnostic Equipment
Fully automated short-term incubation cycle antimicrobial susceptibility system.
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