FLEXIGRIP

Organization name

Praesidia S.r.l.

SRN

IT-MF-000010975

Manufacturer status

Active

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

• Consult instructions for use
• Do not re-use
• Do not use if package is damaged
• Do not use past indicated date
• EUH 208 – Contains (name of sensitising substance). May produce an allergic reaction.

  Ni

• MR SAFE

Primary placement in Italy; available across 13 countries total.

Trade name

FLEXIGRIP

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.

08033675780290

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.

803367578FLEXIGRIPTY

Reference / catalog number

FG0400-1

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 IIb

Applicable legislation

MDR [Regulation (EU) 2017/745 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

• 40 MU50

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

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

• H02010202STERNAL CLIPS

• Class IIb medical devices in EUDAMED

Certificate health across this manufacturer's portfolio.