FREND™ SYSTEM - Indonesia BPOM Medical Device Registration
FREND™ SYSTEM is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 10102320460. The device is manufactured by NANOENTEK INC from Korea, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is SEGMED DISTRIBUTION INDONESIA.
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Risk Classification
Product Class
Kelas : 1
Manufacturer
NANOENTEK INCCountry of Origin
Korea
Authorized Representative
SEGMED DISTRIBUTION INDONESIAAR Address
SEGMED DISTRIBUSI INDONESIA
Registration Date
Mar 22, 2023
Expiry Date
Oct 27, 2025
Product Type
Clinical Laboratory Equipment
Fluorometer for clinical use.
Invitro Diagnostics
FREND TSH Neo
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NANOENTEK Immunoassay Control FD Level 1 & 2
2019 Frend™ Psa Plus. All Rights Reserved.
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