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FOKUS Neurosurgical Instrument - Indonesia BPOM Medical Device Registration

FOKUS Neurosurgical Instrument is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 11002220074. The device is manufactured by CEATEC MEDIZINTECHNIIK GMBH & CO. KG. from Germany, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is PT. FOCUS DIAGNOSTIC INDONESIA.

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 : A
FOKUS Neurosurgical Instrument
Analysis ID: AKL 11002220074

Risk Classification

Kelas Resiko : A

Product Class

Kelas : 1

Country of Origin

Germany

Authorized Representative

PT. FOCUS DIAGNOSTIC INDONESIA

AR Address

Jl. Jatipadang Raya No.9A, RT.6/RW.4, Kelurahan Jatipadang, Kecamatan Pasar Minggu, Kota Jakarta Selatan, DKI Jakarta 12540

Registration Date

Sep 26, 2022

Expiry Date

Sep 18, 2025

Product Type

Surgical Neurology Equipment

Nonpowered neurosurgical instrument.

Non Electromedic Non Sterile

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