LINE EXTENSION PVC WITHOUT DEHP 3X4,1 REGULATEUR DE DÉBIT GRADUE SITE Y LUER LOCK MOBILE FILTRE PURGE

Reference : PMFLVMYFP02

  • Precision rotary flow regulator
  • Luer lock mobile
  • Site Y
  • DEHP-free

Description

Rotary flow regulators have a standardized flow stability of +/- 10% over time (ISO8536-14 standard), and are therefore considered lt;precision lt; regulators.


It should be noted that many factors influence flow regulation (viscosity, height, blood pressure, etc.): drop-counting and regular monitoring are therefore good practice when using these precision regulators.





Extender with :
High-quality tubing: flexible, anti-plication PVC
Precision rotary flow regulator: Smooth, easy adjustment - Constant, reliable flow thanks to graduated rotary flow regulator.
Optimum technical features: Movable Luer Lock tip
Pressure resistance: 4000 hPa (4 Bars - 58 psi)
Dead volume: 4.38ml.

Graduation from 0 to 250 mL/h.

Purging information: graduations are reliable to +/- 20% from 20ml upwards, provided the following purging protocol is followed...:



    • Purge the line while keeping the flow regulator in the lt;open lt; position (delivered in the lt;open lt; position).





    • After purging the line, and before connecting the device to the patient's vascular access, turn the flow regulator to the lt;off lt; position.






Contact us to obtain the correct use sheet.





Contact with 0.5% or 2% Chlorhexidine in 70° Isopropyl alcohol, without evaporation time, while the luer lock is connected, and therefore under physical stress, presents a significant risk of luer lock cracking, and should be avoided wherever possible.

In line with SF2H (2019) recommendations, disinfecting connectors (when necessary) with 70° ethyl alcohol is always preferable, as it is just as effective at disinfecting inert materials, and with much less risk of altering plastics.

Technical
information

Indications 
This medical device is designed for the parenteral administration of injectable preparations (drugs, nutrients). This device enables precise gravity administration of injectable parenteral preparations: drugs, solutions, parenteral nutrition. Do not use with high-risk drugs or drugs with narrow therapeutic margins (catecholamines, morphine, heparin, insulin, potassium chloride, anticancer drugs requiring infusion pump administration, and all pharmaceutical specialties whose R.C.P. includes the need for infusion pump or syringe pump administration). Source : OMEDIT CENTRE -- Les bonnes pratiques de perfusion : Module lt; La précision du débit de perfusion lt;.

Used materials 
Capuchon : PE Luer Lock femelle : PC Tube : PVC Régulateur de débit : ABS / TPE Site d'injection : ABS / Polyisoprène synthétique Luer Lock mâle : ABS Capuchon : PE

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 : 0197
  • EU directive/regulation : DIRECTIVE 93/42/CEE
  • annexe : V

sterile 

  • sterile : yes
  • sterilization method : ethylene oxide

conformity 

  • Small-bore connectors for liquids and gases in healthcare applications - Part 7: Connectors for intravascular or hypodermic applications
  • Infusion equipment for medical use — Part 9: Fluid lines for single use with pressure infusion equipment

Logistics
information

Transport conditions 

Protected from light and humidity

Conditioning Parts quantities Dimensions in cm Weight in kg Ean 13 of conditioning
UNIT 1 21 x 13 x 0 06972620110510
BAG 25 55 x 30 x 5 0.510
CASE 150 39 x 42 x 37 16972620110517

Rotary flow regulators have a standardized flow stability of +/- 10% over time (ISO8536-14 standard), and are therefore considered lt;precision lt; regulators.


It should be noted that many factors influence flow regulation (viscosity, height, blood pressure, etc.): drop-counting and regular monitoring are therefore good practice when using these precision regulators.





Extender with :
High-quality tubing: flexible, anti-plication PVC
Precision rotary flow regulator: Smooth, easy adjustment - Constant, reliable flow thanks to graduated rotary flow regulator.
Optimum technical features: Movable Luer Lock tip
Pressure resistance: 4000 hPa (4 Bars - 58 psi)
Dead volume: 4.38ml.

Graduation from 0 to 250 mL/h.

Purging information: graduations are reliable to +/- 20% from 20ml upwards, provided the following purging protocol is followed...:



    • Purge the line while keeping the flow regulator in the lt;open lt; position (delivered in the lt;open lt; position).





    • After purging the line, and before connecting the device to the patient's vascular access, turn the flow regulator to the lt;off lt; position.






Contact us to obtain the correct use sheet.





Contact with 0.5% or 2% Chlorhexidine in 70° Isopropyl alcohol, without evaporation time, while the luer lock is connected, and therefore under physical stress, presents a significant risk of luer lock cracking, and should be avoided wherever possible.

In line with SF2H (2019) recommendations, disinfecting connectors (when necessary) with 70° ethyl alcohol is always preferable, as it is just as effective at disinfecting inert materials, and with much less risk of altering plastics.

Indications 
This medical device is designed for the parenteral administration of injectable preparations (drugs, nutrients). This device enables precise gravity administration of injectable parenteral preparations: drugs, solutions, parenteral nutrition. Do not use with high-risk drugs or drugs with narrow therapeutic margins (catecholamines, morphine, heparin, insulin, potassium chloride, anticancer drugs requiring infusion pump administration, and all pharmaceutical specialties whose R.C.P. includes the need for infusion pump or syringe pump administration). Source : OMEDIT CENTRE -- Les bonnes pratiques de perfusion : Module lt; La précision du débit de perfusion lt;.

Used materials 
Capuchon : PE Luer Lock femelle : PC Tube : PVC Régulateur de débit : ABS / TPE Site d'injection : ABS / Polyisoprène synthétique Luer Lock mâle : ABS Capuchon : PE

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 : 0197
  • EU directive/regulation : DIRECTIVE 93/42/CEE
  • annexe : V

sterile 

  • sterile : yes
  • sterilization method : ethylene oxide

conformity 

  • Small-bore connectors for liquids and gases in healthcare applications - Part 7: Connectors for intravascular or hypodermic applications
  • Infusion equipment for medical use — Part 9: Fluid lines for single use with pressure infusion equipment

Transport conditions 

Protected from light and humidity

Conditioning Parts quantities Dimensions in cm Weight in kg Ean 13 of conditioning
UNIT 1 21 x 13 x 0 06972620110510
BAG 25 55 x 30 x 5 0.510
CASE 150 39 x 42 x 37 16972620110517

Associated products

LINE EXTENSION PVC WITHOUT DEHP 3X4,1 GRADUAL FLOW REGULATOR LUER LOCK MOBILE BLEED FILTER
LINE EXTENSION PVC WITHOUT DEHP 3X4,1 FLOW REGULATOR GREEN NON GRADUATED LUER LOCK MOBILE FILTER BLEED

Associated products

LINE EXTENSION PVC WITHOUT DEHP 3X4,1 GRADUAL FLOW REGULATOR LUER LOCK MOBILE BLEED FILTER
LINE EXTENSION PVC WITHOUT DEHP 3X4,1 FLOW REGULATOR GREEN NON GRADUATED LUER LOCK MOBILE FILTER BLEED

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