ABX Pentra Reference 280 ml - Indonesia BPOM Medical Device Registration
ABX Pentra Reference 280 ml is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20101520327. The device is manufactured by HORIBA ABX SAS, FRANCE from France, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. HORIBA INDONESIA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
HORIBA ABX SAS, FRANCECountry of Origin
France
Authorized Representative
PT. HORIBA INDONESIAAR Address
Jl. Jalur Sutera , Blok. 20A, No. 16 - 17, Kel. Kunciran, Kec. Pinang
Registration Date
Feb 08, 2025
Expiry Date
Oct 30, 2029
Product Type
Clinical Chemistry Test System
Quality control material (assayed and unassayed) (cair)
Invitro Diagnostics
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