Intended purpose of use: to provide aspiration (suction) to a surgical site and this device is connected to an aspiration device using suction tubing.
Product description:
Suction tube with removable tip and tubing connector used for aspirating fluids/secretions from the operative area.
Material: Austenitic steel (non-quenched, non-magnetic steel).
Austenitic steel composition: 16 to 18% chromium; 10 to 14% nickel; 2 to 3% molybdenum.
Curved.
Length: approx. 280mm.
Diameter: approx. 6mm of 8mm.
Autoclavable
Distal end of the Cannula must be atraumatic
Instructions for use:
Used for aspirating fluids / secretions from the operative area.
Safety process:
This item must be cleaned, disinfected after each use, and sterilised in a steam steriliser.
Supplied with:
Manufacturer's instruction for use. Cleaning, disinfection and sterilization instructions
Packaging and labelling:
Primary packaging:
One (1) Suction Tube in a plastic bag
Secondary packaging: Protected unit.
Ten (10) suction tubes in a box.
Symbols used according ISO 15223
CE Mark
Regulatory & Conformity Requirements:
CE mark Comply to EU Council Directive 93/42/EEC (MDD) of EU Regulations 2017/745 (MDR) with valid EC Certificate and Declaration of Conformity for the CE mark is applicable.
US FDA 510(K) clearance
CE certificate available for Class IIa and above devices
Manufacturer’s Quality Management System is certified to ISO 13485 : 2016
Classification:
Classified under EU MDR 2017/745 as Class I device
Environmental requirements:
ISO 14001
Product description:
Suction tube with removable tip and tubing connector used for aspirating fluids/secretions from the operative area.
Material: Austenitic steel (non-quenched, non-magnetic steel).
Austenitic steel composition: 16 to 18% chromium; 10 to 14% nickel; 2 to 3% molybdenum.
Curved.
Length: approx. 280mm.
Diameter: approx. 6mm of 8mm.
Autoclavable
Distal end of the Cannula must be atraumatic
Instructions for use:
Used for aspirating fluids / secretions from the operative area.
Safety process:
This item must be cleaned, disinfected after each use, and sterilised in a steam steriliser.
Supplied with:
Manufacturer's instruction for use. Cleaning, disinfection and sterilization instructions
Packaging and labelling:
Primary packaging:
One (1) Suction Tube in a plastic bag
Secondary packaging: Protected unit.
Ten (10) suction tubes in a box.
Symbols used according ISO 15223
CE Mark
Regulatory & Conformity Requirements:
CE mark Comply to EU Council Directive 93/42/EEC (MDD) of EU Regulations 2017/745 (MDR) with valid EC Certificate and Declaration of Conformity for the CE mark is applicable.
US FDA 510(K) clearance
CE certificate available for Class IIa and above devices
Manufacturer’s Quality Management System is certified to ISO 13485 : 2016
Classification:
Classified under EU MDR 2017/745 as Class I device
Environmental requirements:
ISO 14001
| Pack Size | Avg. Price |
|---|---|
| Pack of 1 | $11.76 |
