Organization name

ADRANOX SRL

SRN

IT-MF-000027181

Manufacturer status

Active

6 warnings recorded — scroll inside the panel to see all entries.

• H225 – Highly flammable liquid and vapour.
• H319 – Causes serious eye irritation.
• P210 – Keep away from heat/sparks/open flames/hot surfaces. — No smoking.
• P280 – Wear protective gloves/protective clothing/eye protection/face protection.
• P233 – Keep container tightly closed.
• P337 – If eye irritation persists: P313 – Get medical advice/attention.

Primary placement in Germany; available across 28 countries total.

Trade name

EURONDA – SANIFIZER SURFACES

UDI-DI code

Primary DI

The Primary DI is the main UDI-DI a manufacturer designates as the principal identifier for a device in EUDAMED.

08056304411785

Basic UDI-DI

Basic UDI-DI

The Basic UDI-DI is the main identifier that groups together all device variants of the same model — the regulatory "family" key.

805630441LYSONOXSPRAY48ZT

Reference / catalog number

246007

Issuing entity

UDI issuing entities

Issuing entities are the organisations the European Commission has designated to assign Unique Device Identifiers under the EU's UDI system.

GS1

Risk category

MDR risk classes

MDR risk classes rank medical devices from lowest risk (Class I) to highest (Class III), which determines how much regulatory scrutiny they face.

Class IIa

Applicable legislation

MDR [Regulation (EU) 2017/745 on medical devices]

Status

On the market

Quantity

12

Additional product description

—

Additional information URL

https://download.euronda.com/

Clinical sizes

• 750 MU03

• Batch number
• Expiration date
• Manufacturing date
• Serial number
• Software identification

European Medical Device Nomenclature — the EU product classification assigned to this device.

• D99DISINFECTANTS, ANTISEPTICS, STERILISING AGENTS AND DETERGENTS FOR MEDICAL DEVICES - OTHER

• Class IIa medical devices in EUDAMED

No certificate specifically references this device's Basic UDI-DI.