Organization name

ADRANOX SRL

SRN

IT-MF-000027181

Manufacturer status

Active

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

• H319 – Causes serious eye irritation.
• H315 – Causes skin irritation.
• P305 – IF IN EYES: P338 – Remove contact lenses, if present and easy to do. Continue rinsing.
• P305 – IF IN EYES: P351 – Rinse cautiously with water for several minutes.
• P280 – Wear protective gloves/protective clothing/eye protection/face protection.
• P332 – If skin irritation occurs: P313 – Get medical advice/attention.
• P337 – If eye irritation persists: P313 – Get medical advice/attention.
• P302 – IF ON SKIN: P352 – Wash with plenty of soap and water.

Primary placement in Germany; available across 28 countries total.

Trade name

SANIFIZER NEUTRALIZER

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.

08056304410863

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.

805630441LYSONOXWDND--NQA

Reference / catalog number

249006

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 I

Applicable legislation

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

Status

On the market

Quantity

2

Additional product description

—

Additional information URL

https://download.euronda.com/

Clinical sizes

• 5 MU02

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

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

• V0799PRODUCTS FOR CLEANING MEDICAL DEVICES NOT INCLUDED IN OTHER CLASSES - OTHER

• Class I medical devices in EUDAMED

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