AXEL

Organization name

UAB "Medicinos linija"

SRN

LT-MF-000002719

Manufacturer status

Active

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

• CW032

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

  EUDAMED did not publish a description for this code.
• CW083

  EUDAMED did not publish a description for this code.
• CW089

  EUDAMED did not publish a description for this code.
• CW135

  EUDAMED did not publish a description for this code.
• CW148

  EUDAMED did not publish a description for this code.
• CW162

  EUDAMED did not publish a description for this code.
• CW164

  EUDAMED did not publish a description for this code.
• CW167

  EUDAMED did not publish a description for this code.
• CW296

  EUDAMED did not publish a description for this code.
• CW193

  EUDAMED did not publish a description for this code.
• CW415

  EUDAMED did not publish a description for this code.
• CW397

  EUDAMED did not publish a description for this code.
• CW304

  EUDAMED did not publish a description for this code.
• CW422

  EUDAMED did not publish a description for this code.
• CW450

  EUDAMED did not publish a description for this code.
• CW305

  EUDAMED did not publish a description for this code.
• CW401

  EUDAMED did not publish a description for this code.
• CW276

  Product should not be used with other products containing eugenol as eugenol may disturb polymerization process.

Primary placement in Lithuania; available across 32 countries total.

Trade name

AXEL

UDI-DI code

04772178008138

Basic UDI-DI

4772178ML-LCNHC2C

Reference / catalog number

CFC611202

Issuing entity

GS1

Risk category

Class IIa

Applicable legislation

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

Status

On the market

Quantity

1

Additional product description

AXEL is light curing, bioinert, radiopaque nano hybrid composite in Vita* shades with high aesthetics, excellent polishability, colour stability, high strength and abrasion resistance. * Registered trademark of the Vita Zahnfabrik H.Rauter GmbH & Co. KG, Bad Sackingen, Germany.

Additional information URL

https://www.i-dental.lt/eIFU

Clinical sizes

No clinical sizes registered for this device.

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

• Q01010103DENTAL RESTORATIVE COMPOSITES