Organization name

Pikdare S.p.A.

SRN

IT-MF-000010069

Manufacturer status

Active

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

• Consult instructions for use

Primary placement in Italy; available across 18 countries total.

Trade name

Stericompress

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.

08058090048213

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.

805809022885000LN

Reference / catalog number

58022885000000

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

24

Additional product description

—

Additional information URL

No additional information URL provided by the manufacturer.

Clinical sizes

• 70x100cm

1 packaging level registered — each level carries its own UDI-DI.

• 08058090048213× 24 unitsBase unit
  • 58058090048218× 12 units

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

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

• M0201020101COTTON GAUZES, FOLDED, WITHOUT X-RAY DETECTABLE THREAD, STERILE

• Class I medical devices in EUDAMED

Certificate health across this manufacturer's portfolio.

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