2019 Frend™ Psa Plus. All Rights Reserved. - Indonesia BPOM Medical Device Registration
2019 Frend™ Psa Plus. All Rights Reserved. is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20306320227. The device is manufactured by NANOENTEK INC from Korea, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is SEGMED DISTRIBUTION INDONESIA.
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FREND™ PSA Plus
Risk Classification
Product Class
Kelas : 2
Manufacturer
NANOENTEK INCCountry of Origin
Korea
Authorized Representative
SEGMED DISTRIBUTION INDONESIAAR Address
SEGMED DISTRIBUSI INDONESIA
Registration Date
May 25, 2023
Expiry Date
Oct 27, 2025
Product Type
Tumor Antigen Immunologic Test System
Tumor-associated antigen immunological test system.
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