A1-092-619/0S

Organization name

Titanox S.r.l.

SRN

IT-MF-000020325

Manufacturer status

Active

1 warning recorded — scroll inside the panel to see all entries.

• CW999

  Do not use detergents or disinfectants containing chlorides or trichloroethylene, as they may damage the aluminum. Use only suitable filters and comply with their specified service life. Improper use or non-validated sterilization may compromise the sterile barrier and the safety of the contents. The device must be used exclusively by qualified personnel.

Primary placement in Italy; available across 25 countries total.

Trade name

not provided

UDI-DI code

08059304700699

Basic UDI-DI

805930470A04FILTXX

Reference / catalog number

A1-092-619/0S

Issuing entity

GS1

Risk category

Class I

Applicable legislation

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

Status

On the market

Quantity

1

Additional product description

Reusable container made of anodized aluminum for the steam sterilization of medical devices. Equipped with a filtration system and a gasket to maintain the sterile barrier and preserve the sterility of the contents after the sterilization process.

Additional information URL

https://www.titanox.it/

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.

• S0199DEVICES FOR STERILISATION AND PACKAGING (EXCLUDING CAT. D - Z) - OTHER