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OSTEOPORE PCL Scaffold Bone Filler - Indonesia BPOM Medical Device Registration

OSTEOPORE PCL Scaffold Bone Filler is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21003022991. The device is manufactured by OSTEOPORE INTERNATIONAL PTE LTD from Singapore, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. ASIA ACTUAL INDONESIA.

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BPOM Registered
Risk Class Kelas Resiko : C
OSTEOPORE PCL Scaffold Bone Filler
Analysis ID: AKL 21003022991

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Country of Origin

Singapore

Authorized Representative

PT. ASIA ACTUAL INDONESIA

AR Address

PERKANTORAN GANDARIA 8 LANTAI 6 UNIT JL. SULTAN ISKANDAR MUDA KEBAYORAN LAMA UTARA JAKARTA SELATAN

Registration Date

Oct 28, 2022

Expiry Date

Mar 13, 2025

Product Type

Therapeutic Neurology Equipment

Methyl methacrylate for cranioplasty.

Non Electromedic Sterile

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