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CORPULS1 - Indonesia BPOM Medical Device Registration

CORPULS1 is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 30505615369. The device is manufactured by GS ELEKTROMEDIZINISCHE GERร„TE, G. STEMPLE GMBH. from Germany, and is classified as Risk Class Kelas Resiko : D. The authorized representative in Indonesia is PT. SEKARGUNA 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 : D
CORPULS1
Analysis ID: AKL 30505615369

Risk Classification

Kelas Resiko : D

Product Class

Kelas : 3

Country of Origin

Germany

Authorized Representative

PT. SEKARGUNA MEDIKA

AR Address

jl.Ciputat Raya no 14 B.Pondok Pinang

Registration Date

Feb 22, 2023

Expiry Date

Aug 28, 2027

Product Type

Therapeutic Cardiology Equipment

Automated external defibrillator.

Non Radiation Electromedics

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