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EMTEL Defibrillator - Indonesia BPOM Medical Device Registration

EMTEL Defibrillator is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 30505420113. The device is manufactured by EMTEL SLIWA SP. K from Poland, and is classified as Risk Class Kelas Resiko : D. The authorized representative in Indonesia is PT. MAGNIFICENT ALKESINDO.

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
EMTEL Defibrillator
Analysis ID: AKL 30505420113

Risk Classification

Kelas Resiko : D

Product Class

Kelas : 3

Manufacturer

EMTEL SLIWA SP. K

Country of Origin

Poland

Authorized Representative

PT. MAGNIFICENT ALKESINDO

AR Address

Jl. Raya Rw. Bambu No.15 F-H, RT.13/RW.5, Ps. Minggu, Kota Jakarta Selatan, Daerah Khusus Ibukota Jakarta 12520

Registration Date

Sep 04, 2024

Expiry Date

Dec 31, 2027

Product Type

Therapeutic Cardiology Equipment

Automated external defibrillator.

Non Radiation Electromedics

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