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ACTIMOVE PHYSIOPACK - Indonesia BPOM Medical Device Registration

ACTIMOVE PHYSIOPACK is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 11403916829. The device is manufactured by GELLO GMBH GELTECHNIK from Germany, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is 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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BPOM Registered
Risk Class Kelas Resiko : A
ACTIMOVE PHYSIOPACK
Analysis ID: AKL 11403916829

Risk Classification

Kelas Resiko : A

Product Class

Kelas : 1

Country of Origin

Germany

Authorized Representative

ESSITY HYGIENE AND HEALTH INDONESIA

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

Dec 08, 2024

Expiry Date

Mar 22, 2029

Product Type

Therapeutic Physical Health Equipment

Hot or cold disposable pack.

Non Electromedic Non Sterile

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