Organization name

Conmed Corporation

SRN

US-MF-000012663

Manufacturer status

Active

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

• Do not re-use
• Consult instructions for use
• Caution
• Do not use if package is damaged
• MR UNSAFE

Primary placement in Belgium; available across 31 countries total.

Trade name

SPIDER-NET

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.

20653405061479

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.

084585408514D8

Reference / catalog number

0350EN

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

5

Additional product description

Nakao Spider-Net® Retrieval Device 2.5 X 5.5 X 350 cm

Additional information URL

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

Clinical sizes

• 350 MU10
• 2.3 MU50

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

• 20653405061479× 1 unitBase unit
  • 10653405061472× 5 units

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

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

• G0305010202DIGESTIVE ENDOSCOPY, RETRIEVAL BASKET DEVICES, NON-REVOLVING

• Class I medical devices in EUDAMED

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