RIESTER Percussion Hammer - Indonesia BPOM Medical Device Registration

RIESTER Percussion Hammer is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 11001123288. The device is manufactured by RUDOLF RIESTER GMBH from Germany, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is PT. LABORA MANDIRI INDO PRATAMA.

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

RIESTER Percussion Hammer

Analysis ID: AKL 11001123288

Risk Classification

Kelas Resiko : A

Product Class

Kelas : 1

Manufacturer

RUDOLF RIESTER GMBH

Country of Origin

Germany

Authorized Representative

PT. LABORA MANDIRI INDO PRATAMA

AR Address

Jl. C. Simanjuntak No. 47

Registration Date

Jun 10, 2021

Expiry Date

Jun 16, 2025

Product Type

Diagnostic Neurology Equipment

Percussor.

Non Electromedic Non Sterile

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Kelas Resiko : B

RIESTER Percussion Hammer - Indonesia BPOM Medical Device Registration

Risk Classification

Product Class

Manufacturer

Country of Origin

Authorized Representative

AR Address

Registration Date

Expiry Date

Product Type

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