Organization name

Laboratoire Huckert's International

SRN

BE-MF-000024078

Manufacturer status

Active

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

• H315 – Causes skin irritation.
• H317 – May cause an allergic skin reaction.
• H318 – Causes serious eye damage.
• H400 – Very toxic to aquatic life.
• H411 – Toxic to aquatic life with long lasting effects.

Primary placement in Belgium; available across 32 countries total.

Trade name

UMONIUM38® Instruments 125ml

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.

05425037715607

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.

B-05425037715607

Reference / catalog number

PF12513

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 IIb

Applicable legislation

MDD [Directive 93/42/EEC on medical devices]

Status

On the market

Quantity

1

Additional product description

—

Additional information URL

No additional information URL provided by the manufacturer.

Clinical sizes

No clinical sizes registered for this device.

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

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

• D0901AMMONIUM SALTS FOR THE DISINFECTION OF MEDICAL DEVICES

• Class IIb medical devices in EUDAMED

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

Certificate health across this manufacturer's portfolio.