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LAWTON Diagnostic Percussion Hammer Instrument Set - Indonesia BPOM Medical Device Registration

LAWTON Diagnostic Percussion Hammer Instrument Set is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 11001120606. The device is manufactured by LAWTON GMBH & CO., KG. MEDICAL. from Germany, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is PT. GLOBAL JAYA MEDIKA.

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
LAWTON Diagnostic Percussion Hammer Instrument Set
Analysis ID: AKL 11001120606

Risk Classification

Kelas Resiko : A

Product Class

Kelas : 1

Country of Origin

Germany

Authorized Representative

PT. GLOBAL JAYA MEDIKA

AR Address

Jl. Penjernihan 1 No. 38

Registration Date

Jan 29, 2021

Expiry Date

Dec 31, 2023

Product Type

Diagnostic Neurology Equipment

Percussor.

Non Electromedic Sterile

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