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PYXIS 3D Titanium OLlF Cage System Instrument - Indonesia BPOM Medical Device Registration

PYXIS 3D Titanium OLlF Cage System Instrument is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 11303420354. The device is manufactured by GS MEDICAL CO., LTD from Korea, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is FAJAR SELARAS PARTNERS.

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Risk Class Kelas Resiko : A
PYXIS 3D Titanium OLlF Cage System Instrument
Analysis ID: AKL 11303420354

Risk Classification

Kelas Resiko : A

Product Class

Kelas : 1

Country of Origin

Korea

Authorized Representative

FAJAR SELARAS PARTNERS

AR Address

RUKAN PULOGADUNG TRADE CENTRE (PTC) BLOK 8C NOMOR 28-29

Registration Date

Oct 22, 2024

Expiry Date

Jul 13, 2026

Product Type

Surgical Orthopaedic Equipment

Orthopedic manual surgical instrument.

Non Electromedic Non Sterile

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