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ZEISS VISUCAM 224 - Indonesia BPOM Medical Device Registration

ZEISS VISUCAM 224 is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21201611553. The device is manufactured by CARL ZEISS MEDITEC AG. from Germany, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is 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 VISUCAM 224
Analysis ID: AKL 21201611553

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

Germany

Authorized Representative

ELO KARSA UTAMA

AR Address

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

Registration Date

Apr 06, 2022

Expiry Date

May 01, 2025

Product Type

Diagnostic Eye Equipment

Opthalmic camera.

Non Radiation Electromedics

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