HELMER Platelet Agitator - Indonesia BPOM Medical Device Registration
HELMER Platelet Agitator is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20206022603. The device is manufactured by HELMER INC. from United States, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is FRISMED HOSLAB INDONESIA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
HELMER INC.Country of Origin
United States
Authorized Representative
FRISMED HOSLAB INDONESIAAR Address
Ruko Bidex Blok G No. 30-31 Jl. Pahlawan Seribu BSD City, 15321
Registration Date
Apr 20, 2023
Expiry Date
Dec 31, 2025
Product Type
Manual Hematology Equipment
Platelet aggregometer.
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