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KINETEC Shoulder CPM Machine - Indonesia BPOM Medical Device Registration

KINETEC Shoulder CPM Machine is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21403911577. The device is manufactured by KINETEC SAS from France, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is GLOBAL SYSTECH MEDIKA.

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
KINETEC Shoulder CPM Machine
Analysis ID: AKL 21403911577

Risk Classification

Kelas Resiko : A

Product Class

Kelas : 1

Manufacturer

KINETEC SAS

Country of Origin

France

Authorized Representative

GLOBAL SYSTECH MEDIKA

AR Address

Jl. TB Simatupang No.17 RT.011/002 Kel. Susukan, Kec. Ciracas Jakarta Timur

Registration Date

Jul 17, 2023

Expiry Date

May 19, 2028

Product Type

Therapeutic Physical Health Equipment

Powered exercise equipment.

Non Radiation Electromedics

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