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FOCUS Partus Set - Indonesia BPOM Medical Device Registration

FOCUS Partus Set is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 11603911916. The device is manufactured by CEATEC MEDIZINTECHNIK GMBH. 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
FOCUS Partus Set

FOKUS Partus Set

Analysis ID: AKL 11603911916

Risk Classification

Kelas Resiko : A

Product Class

Kelas : 1

Country of Origin

Germany

Authorized Representative

PT. FOCUS DIAGNOSTIC INDONESIA

AR Address

18 Office Park, Tower A, Jl. TB Simatupang No.18 MZ Floor, Unit D1-A/89, Kelurahan Kebagusan

Registration Date

Mar 28, 2022

Expiry Date

Mar 28, 2025

Product Type

Surgical Equipment

Manual surgical instrument for general use.

Non Electromedic Non Sterile

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