ADMR102.50

Organization name

ADRANOX SRL

SRN

IT-MF-000027181

Manufacturer status

Active

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

• CW076

  EUDAMED did not publish a description for this code.
• CW085

  EUDAMED did not publish a description for this code.
• CW106

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

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

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

  EUDAMED did not publish a description for this code.
• CW166

  EUDAMED did not publish a description for this code.

Primary placement in Italy; available across 4 countries total.

Trade name

not provided

UDI-DI code

08056304411396

Basic UDI-DI

805630441LYSONOX----PAAFX

Reference / catalog number

ADMR102.50

Issuing entity

GS1

Risk category

Class IIb

Applicable legislation

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

Status

On the market

Quantity

4

Additional product description

—

Additional information URL

https://adranox.com/

Clinical sizes

• 5 MU02

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

• S9002DEVICES FOR STERILISATION WITH PERACETIC ACID (EXCLUDING CAT. D - Z)