TRITAN 3-WAY STOPCOCK BPA-FREE GREEN VALVE 2 STOPPERS 1 GRIP CAP MOBILE MALE LUER LOCK

Reference : R3LVBPAF

  • BPA-free, lipid-resistant stopcock
  • Rigid blister pack facilitating aseptic gripping of the stopcock
  • Two female green stoppers and a white grip cap

Description

Ergonomics: Large green valve stopcock with arrows indicating the direction of flow, mobile 360° - Reliable and secure: Tip equipped with protective cap - 2 female Luer lock tips equipped with green stopper plugs - mobile male Luer Lock tip equipped with a rotating ring and an opaque white cap - Lipid-resistant.
Pressure resistance tested in a laboratory up to 12,000 hPa (12 bar).
 
Made in India.
 
Contact with 0.5% or 2% Chlorhexidine in 70° Isopropyl alcohol, without evaporation time, and while the luer lock is connected, therefore under physical stress, presents a significant risk of cracking of the luer lock, and should be avoided as much as possible.

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

Technical
information

Indications 
Creation of a third channel on the infusion line. Parenteral administration of drugs and fluids. Use not recommended with radiology injectors. Dispose according to the state member regulation. Advised Practices Always use sterile techniques and wear gloves. Inspect the device for cracks or damage before use. Ensure proper fit and secure connections. Maintain device sterility and integrity. Follow pressure ratings and don't exceed limits. Store the device in a sterile and controlled area. Use appropriate cleaning and sterilization methods. Follow the manufacturer's instructions. Discouraged Practices Avoid touching sterile parts with non-sterile hands. Do not use damaged or broken stopcocks. Avoid over-tightening or under-tightening connections. Do not use with incompatible drugs or fluids. Do not use with excessive pressure or inappropriate settings. Avoid exposing to extreme temperatures or humidity. Avoid improper disposal or reuse of single-use devices. Do not modify the stopcock or misuse it.

Used materials 
HDPE high density polyethylene: Stopcock valve, male and female protective stoppers - Tritan®: Stopcock body, male Luer mobile nut

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 : SGS BELGIUM NV - CE1639
  • EU directive/regulation : 93/42/CEE
  • annexe : II

sterile 

  • sterile : yes
  • sterilization method : ethylene oxide

conformity 

  • Sterilization of medical devices - Requirements for medical devices to be designated lt;STERILE lt; - Part 1: Requirements for terminally sterilized medical devices;
  • Sterilization of health-care products - Ethylene oxide - Part 1 : Requiremnets for the development, validation and routine control of a sterilization process for medical devices
  • Infusion equipment for medical use — Part 10: Accessories for fluid lines for single use with pressure infusion equipment
  • Infusion equipment for medical use - Part 4 : Infusion sets for single use, gravity feed.

Logistics
information

Transport conditions 

Protected from light, humidity and heat

Conditioning Parts quantities Dimensions in cm Weight in kg Ean 13 of conditioning
UNIT 1 4 x 7 x 2 0.006 8906065481629
BOX 50 13 x 17 x 10 0.320 18906065481626
CASE 500 29 x 51 x 18 3.300 58906065481624

Ergonomics: Large green valve stopcock with arrows indicating the direction of flow, mobile 360° - Reliable and secure: Tip equipped with protective cap - 2 female Luer lock tips equipped with green stopper plugs - mobile male Luer Lock tip equipped with a rotating ring and an opaque white cap - Lipid-resistant.
Pressure resistance tested in a laboratory up to 12,000 hPa (12 bar).
 
Made in India.
 
Contact with 0.5% or 2% Chlorhexidine in 70° Isopropyl alcohol, without evaporation time, and while the luer lock is connected, therefore under physical stress, presents a significant risk of cracking of the luer lock, and should be avoided as much as possible.

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

Indications 
Creation of a third channel on the infusion line. Parenteral administration of drugs and fluids. Use not recommended with radiology injectors. Dispose according to the state member regulation. Advised Practices Always use sterile techniques and wear gloves. Inspect the device for cracks or damage before use. Ensure proper fit and secure connections. Maintain device sterility and integrity. Follow pressure ratings and don't exceed limits. Store the device in a sterile and controlled area. Use appropriate cleaning and sterilization methods. Follow the manufacturer's instructions. Discouraged Practices Avoid touching sterile parts with non-sterile hands. Do not use damaged or broken stopcocks. Avoid over-tightening or under-tightening connections. Do not use with incompatible drugs or fluids. Do not use with excessive pressure or inappropriate settings. Avoid exposing to extreme temperatures or humidity. Avoid improper disposal or reuse of single-use devices. Do not modify the stopcock or misuse it.

Used materials 
HDPE high density polyethylene: Stopcock valve, male and female protective stoppers - Tritan®: Stopcock body, male Luer mobile nut

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 : SGS BELGIUM NV - CE1639
  • EU directive/regulation : 93/42/CEE
  • annexe : II

sterile 

  • sterile : yes
  • sterilization method : ethylene oxide

conformity 

  • Sterilization of medical devices - Requirements for medical devices to be designated lt;STERILE lt; - Part 1: Requirements for terminally sterilized medical devices;
  • Sterilization of health-care products - Ethylene oxide - Part 1 : Requiremnets for the development, validation and routine control of a sterilization process for medical devices
  • Infusion equipment for medical use — Part 10: Accessories for fluid lines for single use with pressure infusion equipment
  • Infusion equipment for medical use - Part 4 : Infusion sets for single use, gravity feed.

Transport conditions 

Protected from light, humidity and heat

Conditioning Parts quantities Dimensions in cm Weight in kg Ean 13 of conditioning
UNIT 1 4 x 7 x 2 0.006 8906065481629
BOX 50 13 x 17 x 10 0.320 18906065481626
CASE 500 29 x 51 x 18 3.300 58906065481624

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