Organization name

Conmed Corporation

SRN

US-MF-000012663

Manufacturer status

Active

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

• Consult instructions for use
• Caution
• Do not re-use

Primary placement in Belgium; available across 31 countries total.

Trade name

VENI-GARD

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.

10653405014331

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.

084585408540D9

Reference / catalog number

710-2730B

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

1500

Additional product description

VeniGard SP, I.V. Catheter Dressing

Additional information URL

https://eifu.conmed.com/eifu/

Clinical sizes

No clinical sizes registered for this device.

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

• 10653405014331× 1 unitBase unit
  • 20653405014338× 1,500 units

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

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

• C010199PERIPHERAL I.V. CATHETERS AND CANNULAS - OTHER

• Class I medical devices in EUDAMED

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