HAEMONETICS High Efficiency Post-Process Filter Sy - Indonesia BPOM Medical Device Registration
HAEMONETICS High Efficiency Post-Process Filter Sy is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20209020109. The device is manufactured by HAEMONETICS MANUFACTURING INC. from United States, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is TRANSMEDIC INDONESIA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
HAEMONETICS MANUFACTURING INC.Country of Origin
United States
Authorized Representative
TRANSMEDIC INDONESIAAR Address
PERKANTORAN MENARA ERA UNIT G-01, JL. SENEN RAYA NO. 135-137
Registration Date
Jan 22, 2020
Expiry Date
Nov 07, 2024
Product Type
Products used in the manufacture of blood preparations and preparations of origin and blood
Transfer set.
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