HELMER PC4200-PRO Platelet Incubator - Indonesia BPOM Medical Device Registration
HELMER PC4200-PRO Platelet Incubator is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20209420438. The device is manufactured by HELMER INC from United States, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. FRISMED HOSLAB INDONESIA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
HELMER INCCountry of Origin
United States
Authorized Representative
PT. FRISMED HOSLAB INDONESIAAR Address
Ruko Bidex Blok G No. 30-31 Jl. Pahlawan Seribu BSD City, 15321
Registration Date
Nov 15, 2024
Expiry Date
Dec 31, 2026
Product Type
Products used in the manufacture of blood preparations and preparations of origin and blood
Environmental chamber for storage of platelet concentrate.
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