Manufactured by B. Braun, a medical device manufacturer operating under ISO Certified quality management systems (e.g. ISO 13485).
Intended as a single Use sterile medical device for drug preparation and transfer in clinical settings.
Part of B. Braun’s closed System drug preparation portfolio designed to support aseptic technique and reduce contamination risk.
Manufactured by B. Braun, a medical device manufacturer operating under ISO Certified quality management systems (e.g. ISO 13485).
Intended as a single Use sterile medical device for drug preparation and transfer in clinical settings.
Part of B. Braun’s closed System drug preparation portfolio designed to support aseptic technique and reduce contamination risk.
Needle-free transfer and filling connector
Description
The B. Braun FDC 1000 Fluid Dispensing Connector (Fluid Dispensing connector x 100) is a single-use, needle-free syringe connector designed for safe transfer of sterile liquids, reconstitution of lyophilised medicines and filling of unit-dose syringes from a larger master syringe or container. It features female Luer Lock connections on both sides and separate fluid and air channels to support controlled, closed-system transfer, helping to maintain aseptic technique and minimise contamination risk during drug preparation in hospital, theatre and pharmacy settings.
Bnefits
Needle-free transfer device, reducing needlestick injury risk during drug preparation.
Female Luer Lock connections on both sides for secure, standardised connection to syringes and compatible devices.
Designed for filling unit-dose syringes from a large master syringe, improving efficiency in unit-dose preparation.
Suitable for reconstitution of lyophilised drugs and mixing of two sterile fluids in a closed system.
Separate air and fluid channels enabling automatic fluid transfer and reducing the need for manual pressure balancing.
Single-use, single-dose connector that supports infection prevention and helps maintain aseptic technique.
Large grip flanges for ergonomic handling and easier manipulation, even when wearing gloves.
Compatible with B. Braun Ecoflac plus IV containers and 20 mm medication vials as part of the B. Braun drug preparation system.
Indications
Transfer of sterile solutions between syringes (e.g. from a large master syringe to multiple unit-dose syringes).
Reconstitution of lyophilised medicinal products with diluent using a closed, needle-free connection between containers.
Mixing of two sterile fluids where a Luer-to-Luer needle-free connector is required.
Use in hospital wards, theatres, ICUs and hospital pharmacies for aseptic drug preparation and syringe filling.
Part of closed-system handling of hazardous and non-hazardous medications when used within compatible B. Braun systems.
Female Luer Lock connection on both sides to interface with standard Luer syringes and compatible devices.
Connector body with dedicated fluid and air channels designed for automatic fluid transfer and venting during reconstitution (exact polymer material not publicly specified; typically medical-grade plastic).
Formulation
Medical device type: needle-free fluid dispensing connector / syringe connector.
Configuration: FDC 1000 (Fluid Dispensing Connector) with female Luer Lock connections on both sides.
Function: transfer of liquids between syringes and containers, reconstitution and mixing of sterile solutions.
Design: integrated separate air and fluid channels to support automatic transfer during reconstitution and minimise pressure build-up.
Use: single-use, single-dose device intended for sterile drug preparation procedures.
Supplied sterile (sterilisation method not explicitly stated in public materials).
Packaging
Supplied as FDC 1000 Fluid Dispensing Connectors, 100 pieces per box (REF 415080).
Each connector supplied sterile in individual primary packaging (e.g. peel pouch) within an outer carton (exact primary packaging not fully detailed).
Outer carton labelled with product name, reference code (415080), quantity (100 pcs), brand (B. Braun) and basic identification information.
Intended for professional use within clinical and pharmacy environments; not for retail sale to the general public.
Usage
Verify package integrity and expiry date before use; do not use if packaging is damaged or opened.
Open the sterile pack immediately before use, maintaining aseptic technique.
Connect one female Luer Lock end of the FDC 1000 to the master syringe or source container as directed by local protocol.
Connect the other female Luer Lock end to the unit-dose syringe or receiving syringe.
Use the master syringe plunger to transfer the required volume of liquid into the receiving syringe; the separate air and fluid channels are designed to support automatic fluid transfer and pressure equalisation.
If used for reconstitution of lyophilised products, first connect to the diluent source and vial/container as per the B. Braun drug preparation system instructions, then mix and withdraw into unit-dose syringes as required.
Avoid excessive force on connections; always check that Luer Lock connections are fully engaged and secure before and during use.
After completion of transfer and filling procedures, disconnect the connector and dispose of it immediately as clinical/sharps waste in line with local infection control policies.
Do not reuse or resterilise; the product is strictly single-use and single-dose.
Contraindications
Do not use if the sterile packaging is damaged, opened or expired.
Not intended for reuse or resterilisation; reuse may increase the risk of infection, leakage or device failure.
Not designed for direct patient connection (e.g. not for direct IV line-to-patient use); it is a preparation and transfer device for trained healthcare professionals only.
Do not use with incompatible connectors or devices that do not conform to Luer Lock standards.
Follow institutional policies when using with hazardous drugs; use additional protective equipment where required.
Adverse Effects
No direct patient adverse effects are expected when device is used correctly as it is a drug preparation accessory and not applied directly to the patient.
Potential indirect risks if misused, such as contamination of prepared syringes, inaccurate dosing due to leaks or improper connections, or exposure of staff to hazardous drugs if connections are not secure.
Improper handling or reuse could contribute to infection risk or compromise of sterility of prepared medications.
Storage Conditions
Store in a clean, dry environment at room temperature, away from direct sunlight and excessive heat.
Keep in original packaging until point of use to maintain sterility.
Protect from mechanical damage, crushing or puncturing of sterile pouches.
Observe any specific storage instructions and expiry dates on the manufacturer’s carton and labelling.
Keep out of reach of unauthorised personnel and children.
