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PAJUNK Multistim Sensor Nerve Stimulation - Indonesia BPOM Medical Device Registration

PAJUNK Multistim Sensor Nerve Stimulation is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20402311470. The device is manufactured by PAJUNK MEDIZINTECHNOLOGIE GMBH. from Germany, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is BRIDGE TWO.

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 : B
PAJUNK Multistim Sensor Nerve Stimulation
Analysis ID: AKL 20402311470

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

Germany

Authorized Representative

BRIDGE TWO

AR Address

Petojo Melintang No. 17 Kel. Petojo Selatan, Kec. Gambir Jakarta Pusat

Registration Date

Feb 01, 2021

Expiry Date

Aug 31, 2025

Product Type

Monitoring Anesthesia Equipment

Electrical peripheral nerve stimulator.

Non Radiation Electromedics

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