The Sol-Millennium Medical 100088IM is a SOL-CARE 1ml TB Safety Syringe with a fixed needle. The needle is 25G x 1″ and each case contains 1000 units. This safety syringe is designed to prevent reuse and lower the risk of needlestick injuries. The safety mechanism is activated when the user pulls the needle into the barrel of the syringe after medication delivery. This action covers the needle and locks it, preventing needlestick injuries with a manual retractable needle mechanism.
The syringe has a Low Dead Space design (0.01mL) which reduces waste and allows for more efficient medication delivery. It is ideal for key therapeutic areas, such as allergy and immunization. The syringe has clear, bold graduations for accurate dosing. The No Gap design allows the plunger to be pushed to the zero mark without activating the safety mechanism. The user receives visual and audible confirmation of safety mechanism activation. The patented locking ring design ensures the syringe cannot be reused once the needle is locked within the barrel.
This syringe is designed according to ISO 7886-1 and ISO 23908 standards and is not manufactured with Latex, PVC, and DEHP. The syringe is intended to be used by licensed healthcare professionals (HCP) to inject fluids into, or withdraw fluids from, the body. It is also designed to aid in the prevention of needle stick injuries. Users must be trained by a healthcare professional and follow the Instructions for Use. Failure to follow these instructions could result in serious injury to the patient and/or clinician. The syringe is a sharp object and there is a risk of sharp injuries.
The syringe is easy to use with minimal change in technique. The safety mechanism does not obstruct the view of the needle’s tip. The product allows the exchange of needle after drawing up of medication. The Luer lock safety Syringe is intended to be used with standard hypodermic needles.
The labeling does not contain MRI Safety Information. The device is required to be labeled as not containing natural rubber latex or dry natural rubber (21 CFR 801.437). The device is labeled as “Not made with natural rubber latex”. It is for single-use and prescription use (Rx). It is not an over-the-counter (OTC) product, not a kit, not a combination product, and not a human cell, tissue, or cellular or tissue-based product (HCT/P).
