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LAICA Ultrasonic Humidifier - Indonesia BPOM Medical Device Registration

LAICA Ultrasonic Humidifier is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20403611978. The device is manufactured by LAICA S.P.A. from Italy, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is INNOVATION HEALTHCARE INDONESIA.

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 : B
LAICA Ultrasonic Humidifier
Analysis ID: AKL 20403611978

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Manufacturer

LAICA S.P.A.

Country of Origin

Italy

Authorized Representative

INNOVATION HEALTHCARE INDONESIA

AR Address

Komplek Ruko Permata Kota, Blok Q No. 11 Jl. Pangeran Tubagus Angke No. 170 Kel. Penjagalan, Kec. Penjaringan, Jakarta Utara 14450

Registration Date

Jun 26, 2023

Expiry Date

Mar 31, 2025

Product Type

Therapeutic Anesthesia Equipment

Respiratory gas humidifier.

Non Radiation Electromedics

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