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DALI Medical Devices Ltd.

Israel·IL-MF-000029989

Last updated September 18, 2026

About

Dali Medical Devices focuses on the development of injectable drug delivery technologies – from product concept to commercialization.

From the manufacturer's own website. Source

What DALI Medical Devices Ltd. makes

DALI Medical Devices Ltd. manufactures the SAN-Light, an injectable drug delivery device designed for precise medication administration. The product is tailored for controlled, localized delivery of therapeutic agents in clinical settings.

The company’s portfolio is classified under EU Medical Device Regulation as Class IIa devices and is registered in the EU’s eudamed database. DALI Medical Devices Ltd. is based in Israel.

Written from this company's registered devices by an AI model, and not verified by a human reviewer.

Frequently asked questions

What types of medical devices does DALI Medical Devices Ltd. manufacture?

DALI Medical Devices Ltd. specializes in injectable drug delivery devices. Their current product, the SAN-Light, is designed for precise, controlled administration of medications in clinical environments. This device is tailored for localized delivery of therapeutic agents, ensuring targeted treatment.

Where is DALI Medical Devices Ltd. based?

DALI Medical Devices Ltd. is headquartered in Israel. The company’s location is relevant for understanding its regulatory framework and operational base, particularly in the context of EU medical device compliance.

Which regulatory registries list DALI Medical Devices Ltd.’s devices?

DALI Medical Devices Ltd.’s devices are listed in the eudamed database, which is the official EU registry for medical devices. This inclusion ensures transparency and compliance with EU Medical Device Regulation requirements.

How are DALI Medical Devices Ltd.’s devices classified under EU regulations?

DALI Medical Devices Ltd.’s products, including the SAN-Light, fall under Class IIa classification according to the EU Medical Device Regulation. This classification is determined by factors like the device’s intended use, risk level, and potential impact on patient safety, requiring additional scrutiny and conformity assessments.

AI-generated from registry data and not verified by a human reviewer.

Information

Country
Israel
Address
6, Nahal Harif, Yavne, Israel
Facebook
—
Phone
+972-8-3730080
PRRC Contact
Yana Shmilovitz
EUDAMED SRN
IL-MF-000029989
FDA FEI Number
—
DUNS Number
—

Catalogue (1)

DeviceModel / ReferenceRegistriesClassStatus
SAN-Light PS021.002
EUDAMED
Class IIaActive

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