OTT.KLINIJECT 22G

Organization name

Delta Med SPA

SRN

IT-MF-000027962

Manufacturer status

Active

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

• CW011

  EUDAMED did not publish a description for this code.
• CW001

  EUDAMED did not publish a description for this code.
• CW009

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

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

  EUDAMED did not publish a description for this code.

Primary placement in Germany; available across 1 country total.

Trade name

OTT.KLINIJECT 22G

UDI-DI code

08032248400634

Basic UDI-DI

8032248300007C

Reference / catalog number

3025616

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

Obturators single entry are accessories of IV Catheters produced by Delta Med. They are formed by a shaft having the dimension according to the the Gauge of the IV Catheter to which it is intended to be used. The shaft is connected to luer lock fitting used to connect safely the accessory to the catheter hub. The shaft surface is protected by a plastic protector that covers the entire length of the oburators. The reference size of the Obturators is identified by the Gauge-color code. They are intended to close (obstruct) the internal lumen of the catheter to prevent clots formation and for the momentanous suspension of the treatment.

Additional information URL

No additional information URL provided by the manufacturer.

Clinical sizes

• 22G

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

• A070501CAPS OR OBTURATORS, NON-PERFORABLE