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REFOBACIN Bone Cement R - Indonesia BPOM Medical Device Registration

REFOBACIN Bone Cement R is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 31302914874. The device is manufactured by BIOMET FRANCE from France, and is classified as Risk Class Kelas Resiko : D. The authorized representative in Indonesia is PT. KALMED SEJAHTERA INDONESIA.

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BPOM Registered
Risk Class Kelas Resiko : D
REFOBACIN Bone Cement R
Analysis ID: AKL 31302914874

Risk Classification

Kelas Resiko : D

Product Class

Kelas : 3

Manufacturer

BIOMET FRANCE

Country of Origin

France

Authorized Representative

PT. KALMED SEJAHTERA INDONESIA

AR Address

Jl. TMII Pintu II No. 2, RT 006 RW 004,

Registration Date

Jan 24, 2022

Expiry Date

Dec 08, 2026

Product Type

Prosthetic Orthopedic Equipment

Polymethylmethacrylate (PMMA) bone cement with drug

Non Electromedic Sterile

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