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Vascular Access

Accu-Site | Needle Free Valve

Accu-Site | Needle Free Valve

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Product overview

Needle-free design to help reduce the risk of needlestick injuries • Supports closed-system IV access to minimize contamination risk • Enables safe…

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Product advantages

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Key features

See the specification table for the available product configuration and technical details.

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  • Help choosing the right variant and pack configuration.
  • Certificate and documentation support for your destination market.
  • A volume-based quote from our trade team within two working days.

Specifications

Specifications for Accu-Site | Needle Free Valve
ProductNeedle Free Valve
VariantNot Applicable
PackagingPaper Pouch
Pcs in box100
Shelf life5 years

Features &

Benefits

  • Needle-free design to help reduce the risk of needlestick injuries
  • Supports closed-system IV access to minimize contamination risk
  • Enables safe and efficient fluid administration and flushing
  • Helps reduce blood exposure during access
  • Reliable flow performance with low dead space
  • Leak-resistant construction for secure connections
  • Compatible with standard IV systems and connectors
  • Made from medical-grade materials for safe clinical use
  • Suitable for routine and critical care applications Brand | Product code |

Packaging

| Qty. Inner / Outer ACCU-SITE | 2GPND | Paper Pouch | 100/2000

EO STERILE Accu-Site (Needle-Free Valve) is a closed-system vascular access device designed to enable safe and convenient IV therapy without the use of needles. It supports secure fluid administration, flushing, and medication delivery while helping reduce the risk of contamination, blood exposure, and needlestick injuries. Manufactured from high-quality medical-grade materials, Accu-Site ensures reliable flow performance, leak resistance, and compatibility with standard IV systems for routine and critical care applications. The SPM’s Extension line with/ without Needle-free Valve is a sterile, single-use, Extension line with or without Needle-free Valve. The Extension line is available in single or multi-Way. The multi-way extension line allows the administration of fluids or medications. The extension line with/without needle-free valve is sterilized by ethylene oxide. INTENDED PURPOSE: Extension line is used to extend the infusion line during administration of IV fluid. It also provides a pressure monitoring aid and also enables multi-drug administration. INDICATIONS FOR USE: SPM’s Extension line with/without Needle-free connector is intended use to connection and extension infusion or transfusion sets for administration liquids or medications into the circulation system by using of intravenous catheter and cannula. INTENDED PATIENT POPULATIONS: Extension line with/without Needle-free connector is intended to be used in patients irrespective of age and gender. INTENDED USERS: Extension line with/without Needle-free connector is intended to be used by the trained healthcare professionals including doctors, registered practitioners, and paramedics or nursing staff. INTENDED USE ENVIRONMENT: Extension line with/without Needle-free connector is intended to use in healthcare environments like hospitals and clinics. CLINICAL BENEFITS:

  • The transparent, smooth and kink-resistant PVC tube (latex-free) allows seamless connection
  • 6% taper in luer lock allows connection with a variety of medical devices.
  • The needle free valve ensures the leak-proof drug administration. PRINCIPLE OF OPERATION: The Extension line with/without Needle-free connector allows the extension of the vascular access device like infusion set, cannula, etc. It offers more flexibility and convenience during treatments. The Needle-free/ Luer connector offers leak-proof administration of more than one drug using a standard device like Luer lock/Luer slip syringe. PERFORMANCE CHARACTERSTICS:
  • Interoperability with other vascular access devices like infusion set or IV cannula.
  • Extension line with/without Needle-free valve which allows leak proof administration of IV fluid or medications. MATERIAL USED:
  • Tube – PVC
  • Luer Connector- Poly Carbonate
  • Luer cap- Poly Propylene
  • Slide Clamp – LDPP
  • Needle free valve – Poly Carbonate POTENTIAL COMPLICATIONS: Fluid leakage and cross-contamination, Difficulty turning, Incompatibility with medications, Blockage and obstruction, sterility breakdown, misalignment of ports, Material deterioration, and limited durability in high-pressure. INSTRUCTIONS FOR USE:
  • Step 1. Insert the syringe tip into the valve.
  • Step 2. For securing the connection: o For Luer Slip syringe: Insert and rotate 1/4 turn o For Luer lock syringe: turn syringe clockwise
  • Step 3. Inject or Aspirate the fluid.
  • Step 4. To Disconnect, Remove the luer from the valve by turning counter clockwise. HOW SUPPLIED The Extension line with/without Needle-free valve is supplied in sterile, single-use Paper pouch packaging, complete with instructions for use and necessary accessories (if any). WARNINGS
  • For Professional Use Only: This device must be used only by trained healthcare professionals
  • Sterile

Packaging

: Do not use if the packaging is damaged or opened prior to use.

  • Single Use Only: The device is designed for single use. Do not reuse or resterilize.
  • Proper Handling: Handle with care to avoid damage to the device, which could compromise its sterility and functionality. Allergic Reactions: Check patient history for allergies to materials in the Extension line.
  • Inspect Before Use: Ensure all components are present and undamaged before use
  • Follow Instructions: Carefully follow the included instructions for use to avoid complications
  • Dispose Properly: Dispose of the device in accordance with local regulations for medical waste. PRECAUTIONS:
  • Check the integrity and functionality of the device before use. Do not use if the package is open or damaged.
  • Determine patient’s condition and vitals status during device application / Operation.
  • When handling the product care should be taken to avoid damage from handling. Avoid crushing and crimping damage to the product due to application of surgical instruments such as forceps, etc.
  • Conduct procedure under strict surgical protocol and ensure complete asepsis.
  • Do not Re-sterilize. Do not Re-use.
  • Single use only.
  • Do use after the Expiry Date CAUTIONS:
  • Store in a cool and dry place
  • Discard after single uses
  • Do not use if the package is open or damage
  • Do not store at extreme temperature and humidity
  • Do not use if the protective cap is detached.
  • Always swab the top of the female connector with a sterile 70% IPA, wipe 1 or 2 second and allow to dry for 30 seconds.
  • Do not leave slip luer syringe unattended. STORAGE: Stored at controlled temperature (10-40°C). Do not store at freezing temperature. EXPIRATION PERIOD: The device has a shelf life of 5 years from the date of manufacturing. The product should not be used after the indicated sterility expiration date. RETURN OF DAMAGED PRODUCT: Return the product in its original packing identified by the batch number, purchase information, your reference and reason for return. Please contact your local distributor office regarding product return/exchange. DISPOSAL OF THE USED DEVICE:
  • Disposal of the used product should be done according to hospital procedures, State Regulations, National legislation.
  • Device should be disposed after use on individual patient during a single procedure.
  • Disposal of the packaging material should be done as biomedical waste.
  • Any open packaging should be done as biomedical waste.
  • Leftover products should be disposed as biomedical waste. REPORTING: In case of any adverse events and/or potential threat/ complications that may reasonably by regarded as product related and that were not previously expected in nature, severity or occurrence, contact the manufacturer or authorized representative and competent authority of the member state where the user and/or patient is established.

Instructions for use (eIFU)

Supplied instructions are available in English. Confirm the document matches the selected device variant and current pack before use.

No product-specific IFU PDF for this item was included in the supplied documents.

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