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SCHILLER Defibrillator - Indonesia BPOM Medical Device Registration

SCHILLER Defibrillator is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 30505125204. The device is manufactured by SCHILLER MEDICAL SAS from France, and is classified as Risk Class Kelas Resiko : D. The authorized representative in Indonesia is MULYA HUSADA JAYA.

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Risk Class Kelas Resiko : D
SCHILLER Defibrillator

SCHILLER Defibrilator

Analysis ID: AKL 30505125204

Risk Classification

Kelas Resiko : D

Product Class

Kelas : 3

Country of Origin

France

Authorized Representative

MULYA HUSADA JAYA

AR Address

JALAN KERINCI NO. 2-A

Registration Date

Nov 24, 2023

Expiry Date

Oct 31, 2025

Product Type

Therapeutic Cardiology Equipment

Automated external defibrillator.

Non Radiation Electromedics

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