PULSAR Expandable Cage System - Indonesia BPOM Medical Device Registration

PULSAR Expandable Cage System is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21302420120. 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.

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BPOM Registered

Risk Class Kelas Resiko : C

PULSAR Expandable Cage System

Analysis ID: AKL 21302420120

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Manufacturer

GS MEDICAL CO., LTD.

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 29, 2024

Expiry Date

Jul 13, 2026

Product Type

Prosthetic Orthopedic Equipment

Intervertebral body fusion device

Non Electromedic Non Sterile

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PULSAR Expandable Cage System - Indonesia BPOM Medical Device Registration

Risk Classification

Product Class

Manufacturer

Country of Origin

Authorized Representative

AR Address

Registration Date

Expiry Date

Product Type

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