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LEONI PLUS Intensive Care Ventilator - Indonesia BPOM Medical Device Registration

LEONI PLUS Intensive Care Ventilator is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20403810021. The device is manufactured by WILAMED GMBH. from Germany, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is MULTIPURPOSE CIPTASENTOSA.

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BPOM Registered
Risk Class Kelas Resiko : C
LEONI PLUS Intensive Care Ventilator
Analysis ID: AKL 20403810021

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Manufacturer

WILAMED GMBH.

Country of Origin

Germany

Authorized Representative

MULTIPURPOSE CIPTASENTOSA

AR Address

Surapati Core Blok M No.1 Jl. Phh. Mustofa No. 39 Bandung 022-87241400

Registration Date

Jul 20, 2023

Expiry Date

May 04, 2026

Product Type

Therapeutic Anesthesia Equipment

Continuous ventilator.

Non Radiation Electromedics

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