Organization name

Conmed Corporation

SRN

US-MF-000012663

Manufacturer status

Active

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

• Do not re-use
• Contains hazardous substances
• Do not resterilize
• Do not use if package is damaged
• Consult instructions for use
• Caution

Primary placement in Belgium; available across 32 countries total.

Trade name

Infinity AIM™

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.

20845854649913

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.

084585408696E9

Reference / catalog number

KSC20

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 IIa

Applicable legislation

MDR [Regulation (EU) 2017/745 on medical devices]

Status

On the market

Quantity

1

Additional product description

Infinity AIM Suture Cutter and Skid

Additional information URL

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

Clinical sizes

No clinical sizes registered for this device.

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

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

• H900899SINGLE-USE INSTRUMENTS FOR SUTURES - OTHER

• Class IIa medical devices in EUDAMED

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