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The DEHP-free, BPA-free INFINEED lt;Gravity lt; 1-way infusion set has been designed to minimise the device's environmental impact. Two methods have been used: first, by reducing the plastic mass used by around 10%, without making any changes to functionality; second, by exclusively using raw materials that are free from endocrine disruptors (elimination of components comprising DEHP or BPA.)
The Y-site enables the bypass delivery of bolus drugs using a syringe and needle.
Infuser with:
- Two-channel perforator
- Air intake: Delivered closed for immediate use on a 0.2µ filter bag
- Chamber: 5.5 mL / 5 cm long - Flexible and transparent, Calibrated at 20 drops = 1ml ± 0.1ml, 15µ particle filter.
- Flow regulator: ABS linear flow control for good roller clamp rigidity, precision and reliability.
- Tubing: PVC (DINCH) designed for comfort, optimal flow adjustment consistency and to prevent kinks.
- Latex-free Y-site made from synthetic polyisoprene
- End fitting: Mobile Luer Lock,
- End stopper equipped with a purge filter with anti-bacterial membrane of 0.8µm. Very pressure-resistant purge filter.
Length: 160cm
Residual volume: 16.5 ml
Made in China
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
This device enables the parenteral administration by gravity of injectable preparations: parenteral drugs, solutions and nutrition.
According to good perfusion practice, the infusion line can remain in place for up to 96 hours (CODIMS, OMEDIT CENTRE-VAL-DE-LOIRE, Socle de connaissance de la perfusion - SFAR, EUROPHARMAT, [...]).
In addition, the SF2H reminds us not to change the main infusion line before 4 days, without exceeding 7 days.
This device has been tested for pressure, traction and lipid resistance for up to 7 days.
The length of time the infusion line should be maintained should be discussed and validated in each facility, in order to establish an internal protocol.
Dispose according to legislation in member state.
Used materials
PVC (DEHP< 01.% (m/>)): Chamber, air intake, tubing - DINCH: plasticiser - Polyethylene: Purge filter, protective cap for perforator, mobile Luer Lock - Acrylonitrile Butadiene Styrene: Perforator, linear flow regulator - Polyamide: Particle filter - Injection site: ABS + synthetic polyisoprene
Labeling
on each unit are written the reference, the lot/serial number, the sterilization method and the expiry date if applicable
medical device
sterile
conformity
economic operator
Transport conditions
Protected from light, humidity and heat
| Conditioning | Parts quantities | Dimensions in cm | Weight in kg | Ean 13 of conditioning |
| UNIT | 1 | 21 x 10 x 1 | 3661809029349 | |
| BOX | 25 | 3661809129346 | ||
| CASE | 250 | 59 x 39 x 27 | 3661809329340 | |
| PALLET | 6000 |