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SEBIA Normal Control Serum - Indonesia BPOM Medical Device Registration

SEBIA Normal Control Serum is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20101220064. The device is manufactured by SEBIA from France, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is EN. RIOCA MEDICA.

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Risk Class Kelas Resiko : B
SEBIA Normal Control Serum

SEBIA Serum De Controle Normal

Analysis ID: AKL 20101220064

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Manufacturer

SEBIA

Country of Origin

France

Authorized Representative

EN. RIOCA MEDICA

AR Address

Komplek Pesona Indah Kapuk Blok A6 Jl. Kapuk Kamal Raya Kav. 20A

Registration Date

Jan 17, 2022

Expiry Date

Dec 31, 2024

Product Type

Clinical Chemistry Test System

Quality control material (assayed and unassayed) (cair)

Invitro Diagnostics

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