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SEBIA Hydragel β1- β2 15 / 30 - Indonesia BPOM Medical Device Registration

SEBIA Hydragel β1- β2 15 / 30 is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20101220149. 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 Hydragel β1- β2 15 / 30

SEBIA Hydragel β1- β2 15 / 30

Analysis ID: AKL 20101220149

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

Feb 05, 2022

Expiry Date

Dec 31, 2024

Product Type

Clinical Chemistry Test System

Protein (fractionation) test system (kit & cair)

Invitro Diagnostics

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