Organization name

Will-Pharma BV

SRN

NL-MF-000006884

Manufacturer status

Active

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

• Do not re-use
• Consult instructions for use
• Contains biological material of animal origin
• Do not resterilize
• Do not use if package is damaged

Primary placement in Belgium; available across 15 countries total.

Trade name

Willospon®

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.

08712691209205

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-08712691209205

Reference / catalog number

20925NL-1

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 III

Applicable legislation

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

Status

On the market

Quantity

1

Additional product description

Willospon® Gelatin Sponge is a sterile gelatin sponge from porcine origin, insoluble in water, easy to handle, re-absorbable and which can be cut to the desired size without crumbling.

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.

• M040503GELATINE SPONGE HAEMOSTATIC DRESSINGS

• Class III medical devices in EUDAMED

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