LAICA Ultrasonic Nebulizer - Indonesia BPOM Medical Device Registration
LAICA Ultrasonic Nebulizer is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20403514553. 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.
Risk Classification
Product Class
Kelas : 2
Manufacturer
LAICA S.P.A.Country of Origin
Italy
Authorized Representative
INNOVATION HEALTHCARE INDONESIAAR 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 21, 2023
Expiry Date
Mar 31, 2025
Product Type
Therapeutic Anesthesia Equipment
Nebulizer.
Non Radiation Electromedics
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