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PYXIS 3D Titanium PLIF Cage (Sterile) - Indonesia BPOM Medical Device Registration

PYXIS 3D Titanium PLIF Cage (Sterile) is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21302320855. The device is manufactured by GS MEDICAL CO., LTD from Korea, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. FAJAR SELARAS PARTNERS.

This page provides comprehensive regulatory information including complete registration details, manufacturer information, authorized representative details, product classification, and related products. Pure Global AI offers free access to 67,600+ Indonesia medical device registrations, helping global MedTech companies identify partners, analyze markets, and discover business opportunities efficiently.

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BPOM Registered
Risk Class Kelas Resiko : C
PYXIS 3D Titanium PLIF Cage (Sterile)
Analysis ID: AKL 21302320855

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Country of Origin

Korea

Authorized Representative

PT. FAJAR SELARAS PARTNERS

AR Address

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

Registration Date

Jul 02, 2024

Expiry Date

Jul 13, 2026

Product Type

Prosthetic Orthopedic Equipment

Intervertebral body fusion device

Non Electromedic Sterile

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