QUASAR Stand-alone ACIF Cage - Indonesia BPOM Medical Device Registration

QUASAR Stand-alone ACIF Cage is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21302320975. 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

QUASAR Stand-alone ACIF Cage

Analysis ID: AKL 21302320975

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

Komplek Rukan PTC Blok 8C No. 28-29 Pulogadung Tel. 021-46827776 Fax. 021-46827033

Registration Date

Dec 07, 2023

Expiry Date

Jul 13, 2026

Product Type

Prosthetic Orthopedic Equipment

Intervertebral body fusion device

Non Electromedic Non Sterile

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QUASAR Stand-alone ACIF Cage - 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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