AFI LISA Centrifuge Refrigerated - Indonesia BPOM Medical Device Registration
AFI LISA Centrifuge Refrigerated is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 10205420058. The device is manufactured by CENTRIFUGE FIRE from France, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is PT. MEDQUEST GLOBAL PARTNERS.
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Risk Classification
Product Class
Kelas : 1
Manufacturer
CENTRIFUGE FIRECountry of Origin
France
Authorized Representative
PT. MEDQUEST GLOBAL PARTNERSAR Address
MENARA SALEMBA LANTAI 7, JALAN SALEMBA RAYA NOMOR 5-5A
Registration Date
Mar 22, 2024
Expiry Date
Jul 18, 2025
Product Type
Automatic and Semi-Automatic Hematology Equipment
Microsedimentation centrifuge.
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