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ZEAGR Reflex Hammer - Indonesia BPOM Medical Device Registration

ZEAGR Reflex Hammer is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 11001020574. The device is manufactured by HEILEMED TECHNOLOGY GMBH. from Germany, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is PT. MULTIGUNA CIPTASENTOSA.

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
ZEAGR Reflex Hammer
Analysis ID: AKL 11001020574

Risk Classification

Kelas Resiko : A

Product Class

Kelas : 1

Country of Origin

Germany

Authorized Representative

PT. MULTIGUNA CIPTASENTOSA

AR Address

Surapati Core Blok M No.1 Jl. Phh. Mustofa No. 39 Bandung 022-87241400

Registration Date

Feb 21, 2020

Expiry Date

Feb 27, 2024

Product Type

Diagnostic Neurology Equipment

Percussor.

Non Electromedic Non Sterile

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