20g BD Angiocath Peripheral Venous Cannula 48mm 42 mL/min

20g BD Angiocath Peripheral Venous Cannula 48mm 42 mL/min | Product Description

The BD Angiocath™ 20G Peripheral Venous Cannula is designed for peripheral intravenous access in professional healthcare environments. It forms part of the BD Angiocath™ range of peripheral IV catheters and is intended for use by appropriately trained healthcare professionals.

The cannula has a 20G gauge and features a 48mm catheter length, providing a configuration suitable for appropriate peripheral vascular access procedures. The 20G size is identified by its pink colour-coded hub, allowing convenient gauge identification during clinical preparation and use.

This BD Angiocath™ cannula provides a gravity flow rate of 42 mL/min. The catheter is manufactured from FEP (fluorinated ethylene propylene), a material commonly used in peripheral intravenous catheter construction.

The device incorporates a transparent flash chamber to assist with visual confirmation of blood flashback during appropriate catheter placement procedures. Its single-use design supports established infection prevention and clinical handling procedures.

The cannula is intended for use within professional healthcare environments such as hospitals, clinics, emergency departments and other appropriate clinical settings where peripheral intravenous access is performed.

Key Features:

• 20G peripheral venous cannula
• 48mm catheter length
• 42 mL/min gravity flow rate
• Pink colour-coded hub
• FEP catheter material
• Transparent flash chamber
• Designed for peripheral intravenous access
• Sterile, single-use device
• BD Angiocath™ range
• Manufacturer reference: 381137
• Box quantity: 50

The BD Angiocath™ 20G Peripheral Venous Cannula should be used, handled and disposed of according to the manufacturer's instructions and applicable local clinical procedures.

At UKMEDI, we supply a wide range of high-quality medical, healthcare, and hygiene products to customers across the UK. Please follow product instructions and local guidance when using any medical device or healthcare product.