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ZEISS CIRRUS HD-OCT - Indonesia BPOM Medical Device Registration

ZEISS CIRRUS HD-OCT is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21201021285. The device is manufactured by CARL ZEISS MEDITEC., INC from United States, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. ELO KARSA UTAMA.

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BPOM Registered
Risk Class Kelas Resiko : B
ZEISS CIRRUS HD-OCT
Analysis ID: AKL 21201021285

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

United States

Authorized Representative

PT. ELO KARSA UTAMA

AR Address

Jl. Raya Kebayoran Lama No. 34-E, Grogol Selatan, Kebayoran Lama.

Registration Date

Mar 19, 2020

Expiry Date

Sep 30, 2024

Product Type

Diagnostic Eye Equipment

Ophthalmoscope.

Non Radiation Electromedics

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