PCG08NB1TG

Organization name

DBM SRL

SRN

IT-MF-000017565

Manufacturer status

Active

Certificate health across this manufacturer's portfolio.

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

• CW010

  PRECAUTIONS • Do not administer via intravenous route directly. • Do not use the product for purposes other than its intended use. • Do not use the product if the packaging is open or damaged, if the syringe is not fully intact or if the cap is damaged in such a way as to cause leakage from the syringe. • Do not use the product if the solution is not colourless or contains visible particulate matter. • Once opened, the device must be used immediately and disposed of after use. • For single use only. Dispose of any partially used product, the reuse of which could cause cross contamination between patient and operator. • Do not resterilise. Resterilisation carries a risk of cross infection for the patient and/or user. • Do not draw air into the syringe and do not allow air to be trapped in the fluid path. • Use only with compatible Luer adapters.

Primary placement in Italy; available across 1 country total.

Trade name

not provided

UDI-DI code

38056209661989

Basic UDI-DI

805620966DBMWATERFLUSHDB

Reference / catalog number

PCG08NB1TG

Issuing entity

GS1

Risk category

Class I

Applicable legislation

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

Status

On the market

Quantity

200

Additional product description

—

Additional information URL

https://www.dbmitalia.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.

• A02010799PREFILLED SYRINGES - OTHER