Vulnamin PWD

Organization name

Professional Dietetics S.p.A.

SRN

IT-MF-000036312

Manufacturer status

Active

1 warning recorded — scroll inside the panel to see all entries.

• Do not use in the event of known hypersensitivity to the ingredients. There are no known cases of overdose. There are no known side effects. There are no known interactions with drugs and medicinal substances. Although no secondary effects are known during pregnancy and lactation, in these cases the product should only be used after consulting a doctor. VULNAMIN PWD is a well-tolerated product, however local reactions may rarely occur due to hypersensitivity that will resolve spontaneously. However, it is advisable to consult a doctor in the event of concomitant pharmacological treatments and/or treatments being used for more than six weeks.

  OTHER

Primary placement in Poland; available across 10 countries total.

Trade name

Vulnamin PWD

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.

08021756001655

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-08021756001655

Reference / catalog number

D0543

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

• 1 MU24

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

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

• M040499DRESSINGS FOR WOUNDS, SORES AND ULCERATIONS - OTHER

• Class IIb medical devices in EUDAMED

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