2120

Organization name

Innoventa Medica ApS

SRN

DK-MF-000013980

Manufacturer status

Active

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

• CW001

  EUDAMED did not publish a description for this code.
• CW007

  EUDAMED did not publish a description for this code.
• CW011

  EUDAMED did not publish a description for this code.
• CW010

  EUDAMED did not publish a description for this code.
• CW025

  EUDAMED did not publish a description for this code.

Primary placement in Denmark; available across 15 countries total.

Trade name

not provided

UDI-DI code

05745000321049

Basic UDI-DI

5745000321LecigonPEG4N

Reference / catalog number

2120

Issuing entity

GS1

Risk category

Class IIb

Applicable legislation

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

Status

On the market

Quantity

1

Additional product description

—

Additional information URL

https://www.innoventamedica.com/lecigon-peg

Clinical sizes

• 20 MU170

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

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

• G02020201GASTROSTOMY, TUBES AND SETS

Certificate health across this manufacturer's portfolio.