KUBOTA 9920 Large Capacity Refrigerated Centrifuge - Indonesia BPOM Medical Device Registration
KUBOTA 9920 Large Capacity Refrigerated Centrifuge is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20209700462. The device is manufactured by KUBOTA MANUFACTURING CORPORATION. from Japan, 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
KUBOTA MANUFACTURING CORPORATION.Country of Origin
Japan
Authorized Representative
PT. FRISMED HOSLAB INDONESIAAR Address
- Ruko Bidex Blok G No. 30-31 Komplek CBD – BSD City Tangerang 15321 - Pergudangan Tekno Blok G3 No. 26 BSD City, Tangerang
Registration Date
Sep 01, 2021
Expiry Date
Jul 12, 2026
Product Type
Products used in the manufacture of blood preparations and preparations of origin and blood
Automated cell-washing centrifuge for immuno-hematology.
Invitro Diagnostics
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