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QUBE PRO (Phacoemulsification Anterior Vitrectomy) - Indonesia BPOM Medical Device Registration

QUBE PRO (Phacoemulsification Anterior Vitrectomy) is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21203420098. The device is manufactured by FRITZ RUCK OPTHALMOLOGISCHE SYSTEME GMBH from Germany, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. EAST RAYA LESTARI.

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BPOM Registered
Risk Class Kelas Resiko : C
QUBE PRO (Phacoemulsification Anterior Vitrectomy)
Analysis ID: AKL 21203420098

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Country of Origin

Germany

Authorized Representative

PT. EAST RAYA LESTARI

AR Address

Jl. Rawa Kepiting No. 4, Kawasan Industri Pulogadung

Registration Date

Jul 02, 2024

Expiry Date

Feb 01, 2029

Product Type

Surgical Eye Equipment

Phacofragmentation system.

Non Radiation Electromedics

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