TWO-WAY VALVE - POLYCARBONATE - SILICONE - TRANSPARENT - NEUTRAL FLUSH

Reference : EL200

<ul><li>Sterile</li><li>Female luer lock/male luer lock connection</li><li>Flush Neutral<br></li></ul>

Description

Bidirectional valve allowing the administration of medications and/or the collection of blood derivatives (patented design): - Maintenance of asepsis by automatic closure. - No risk of needlestick or contamination for the patient or caregiver. - Improved ergonomics: direct access without plugs.<br>In all cases, the valve septum must be disinfected before each connection with another DM.<br><br>Reliable and secure: System with double seal, no metal components (compatible with MRI).<br><br>Lipid-Resistant: A static test was carried out over a period of 7 days with a 20% lipid emulsion.<br><br>Compatibility: Possible use of alcohol-based antiseptic.<br><br>Neutral flush: Maximum negative displacement: 0.008 ml.<br>Usage Time: The usage time must not exceed 72 hours on a central channel and 96 hours on a peripheral channel or 200 activations.<br>Average flow: &gt;125 ml/min (under a water column of 100 cm)<br>Minimum flow rate: 100ml/min (under a water column of 100 cm) Resistance to retrograde pressure: 2.60 bars. Maximum injection pressure: 325 PSI / 22 bars for a maximum injection flow rate of 10 ml/ sec. Neutral displacement valve, very low fluid displacement when disconnecting the male luer tip: 0.004 ml.<br>Dead volume: 0.04 ml.<br>Duration of use: lipid-resistant 7 days - Do not exceed 400 activations. Total length 2.8cm.<br>

Technical
information

Indications 
This product is intended to inject and circulate liquids to other medical devices.

Used materials 
POM guide ring. Transparent SI key. Transparent PC body. Cannula in transparent lipid-resistant PC.

Labeling 
on each unit are written the reference, the lot/serial number, the sterilization method and the expiry date if applicable

medical device 

  • MD class : IIa
  • MD notified body : 0459
  • EU directive/regulation : 93/42/CEE - 2007/47/CEE
  • annexe : V

sterile 

  • sterile : yes
  • sterilization method : ethylene oxide

conformity 

  • Sterilization of health-care products - Ethylene oxide - Requiremnets for the development, validation and routine control of a sterilization process for medical devices
  • Medical devices - Symbols to be used with medical device labels, labelling and information to be supplied - Part 1: General requirements

Logistics
information

Transport conditions 

Protected from light, humidity and at a temperature between 5 and 40 ° C

Conditioning Parts quantities Dimensions in cm Weight in kg Ean 13 of conditioning
UNIT 1 3661809038259
BOX 200 37 x 11 x 10 3661809038266
CASE 1600 59 x 39 x 44 3661809038273

Bidirectional valve allowing the administration of medications and/or the collection of blood derivatives (patented design): - Maintenance of asepsis by automatic closure. - No risk of needlestick or contamination for the patient or caregiver. - Improved ergonomics: direct access without plugs.<br>In all cases, the valve septum must be disinfected before each connection with another DM.<br><br>Reliable and secure: System with double seal, no metal components (compatible with MRI).<br><br>Lipid-Resistant: A static test was carried out over a period of 7 days with a 20% lipid emulsion.<br><br>Compatibility: Possible use of alcohol-based antiseptic.<br><br>Neutral flush: Maximum negative displacement: 0.008 ml.<br>Usage Time: The usage time must not exceed 72 hours on a central channel and 96 hours on a peripheral channel or 200 activations.<br>Average flow: &gt;125 ml/min (under a water column of 100 cm)<br>Minimum flow rate: 100ml/min (under a water column of 100 cm) Resistance to retrograde pressure: 2.60 bars. Maximum injection pressure: 325 PSI / 22 bars for a maximum injection flow rate of 10 ml/ sec. Neutral displacement valve, very low fluid displacement when disconnecting the male luer tip: 0.004 ml.<br>Dead volume: 0.04 ml.<br>Duration of use: lipid-resistant 7 days - Do not exceed 400 activations. Total length 2.8cm.<br>

Indications 
This product is intended to inject and circulate liquids to other medical devices.

Used materials 
POM guide ring. Transparent SI key. Transparent PC body. Cannula in transparent lipid-resistant PC.

Labeling 
on each unit are written the reference, the lot/serial number, the sterilization method and the expiry date if applicable

medical device 

  • MD class : IIa
  • MD notified body : 0459
  • EU directive/regulation : 93/42/CEE - 2007/47/CEE
  • annexe : V

sterile 

  • sterile : yes
  • sterilization method : ethylene oxide

conformity 

  • Sterilization of health-care products - Ethylene oxide - Requiremnets for the development, validation and routine control of a sterilization process for medical devices
  • Medical devices - Symbols to be used with medical device labels, labelling and information to be supplied - Part 1: General requirements

Transport conditions 

Protected from light, humidity and at a temperature between 5 and 40 ° C

Conditioning Parts quantities Dimensions in cm Weight in kg Ean 13 of conditioning
UNIT 1 3661809038259
BOX 200 37 x 11 x 10 3661809038266
CASE 1600 59 x 39 x 44 3661809038273

Associated products

TWO-WAY VALVE POLYCARBONATE SILICONE TRANSPARENT FLUSH NEUTRAL

Associated products

TWO-WAY VALVE POLYCARBONATE SILICONE TRANSPARENT FLUSH NEUTRAL

Request for technical documentation

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