PT INNOVATION HEALTHCARE INDONESIA

30+

Years of Excellence Italian Healthcare Technology

Ministry of Health RI Certified

CE & ISO Certified

European Technology,
Trusted Quality

LAICA is an Italian healthcare equipment brand with over 30 years of experience delivering high-quality home healthcare products. Every product is designed to strict medical standards and has undergone international clinical testing to ensure accuracy, safety, and user comfort.

High Precision Technology

Advanced sensors with clinically validated measurement accuracy for results you can rely on.

Official Distribution License

All products are officially registered with the Ministry of Health RI (AKL), ensuring safe and legal use in Indonesia.

Easy Home Use

Ergonomic design and intuitive interface allow all family members to use devices independently.

International Standards

Compliant with CE Mark, ISO 13485, and European medical device regulations for guaranteed quality and safety.

From Factory to Your Hands

Every LAICA product we distribute goes through a rigorous selection process, official registration, and quality control before reaching consumers across Indonesia.

Product Selection

LAICA products are selected based on international medical quality standards and Indonesian market needs.

Ministry of Health Registration

Each product is officially registered with the Ministry of Health RI and receives a verified AKL number.

Quality Control

Comprehensive inspection of every product unit according to ISO standards to ensure optimal performance.

Safe Packaging

Products are hygienically packaged with complete manual documentation and official warranty included.

National Distribution

Delivery to pharmacies, clinics, hospitals, and direct consumers throughout all regions of Indonesia.

Internationally Recognized

All LAICA products distributed by PT Innovation Healthcare Indonesia meet international certification standards and are officially registered with the Ministry of Health of the Republic of Indonesia.

CE Mark

Conformite Europeenne — meets European Union safety and performance standards for medical devices.

ISO 13485

Medical device quality management system — guaranteeing consistency and production safety.

Ministry of Health License

Officially registered with the Ministry of Health RI with publicly verifiable AKL numbers.

Medical Device Directive

Full compliance with medical device directive 93/42/EEC as a Class II medical device.