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ACTIMOVE Lumbar - Indonesia BPOM Medical Device Registration

ACTIMOVE Lumbar is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 11402310097. The device is manufactured by DONGGUAN PARK SPORT PRODUCTS CO. LTD. from China, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is PT. ESSITY HYGIENE AND HEALTH 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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Risk Class Kelas Resiko : A
ACTIMOVE Lumbar

ACTIMOVE Lumbal

Analysis ID: AKL 11402310097

Risk Classification

Kelas Resiko : A

Product Class

Kelas : 1

Country of Origin

China

AR Address

Green Office Park 6, Wing B, lantai 1, Zona 8-12, BSD Green Office Park, BSD City, Desa Sampora, Kec. Cisauk, Kab.Tangerang 15345

Registration Date

Nov 13, 2020

Expiry Date

May 16, 2025

Product Type

Prosthetic Physical Health Equipment

Truncal orthosis.

Non Electromedic Non Sterile

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