Organization name

MedOne Surgical, Inc.

SRN

US-MF-000002763

Manufacturer status

Active

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

• Do not re-use
• Do not use if package is damaged

Primary placement in Austria; available across 30 countries total.

Trade name

Backflush FlexTip™ 23g

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.

00811313012907

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.

081131301MEDSURG01QY

Reference / catalog number

3290

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

Sterile Cannula Family

Additional information URL

https://www.medone.com/

Clinical sizes

• 23 gauge

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

• 00811313012907× 1 unitBase unit
  • 10811313012904× 5 units

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

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

• Q021101OCCULAR IRRIGATION AND ASPIRATION CANNULAS, SINGLE-USE

• Class IIa medical devices in EUDAMED

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

Certificate health across this manufacturer's portfolio.