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ZEISS CIRRUS HD-OCT 5000 - Indonesia BPOM Medical Device Registration

ZEISS CIRRUS HD-OCT 5000 is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21201719346. The device is manufactured by FLEXTRONICS MANUFACTURING ( SINGAPORE ) PTE., LTD. from Singapore, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. ELO KARSA UTAMA.

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 : B
ZEISS CIRRUS HD-OCT 5000
Analysis ID: AKL 21201719346

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

Singapore

Authorized Representative

PT. ELO KARSA UTAMA

AR Address

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

Registration Date

Sep 06, 2021

Expiry Date

May 01, 2025

Product Type

Diagnostic Eye Equipment

Ophthalmoscope.

Non Radiation Electromedics

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