BD 305215 Nokor Admix Needles Thin 18 Gauge 1.5 Inch 1000/CS
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Description
BD 305215 Nokor Admix Needles Thin 18 Gauge 1.5 Inch 1000/CS
305215 – 18 G BD Nokor Admix Needle 1 1/2 in. Thin wall, Sterile, Single use
The BD Nokor needle design features a cannula side port to place fluid on the side wall of a container during reconstitution. Some drug manufacturers recommend this to help reduce foaming or spray of powdered medication.
- BD Nokor design eliminates clogged cannula, retaining venting capability
- Vented needles available, designed to reduce internal container pressure
Key Product Features
| Hub Color | Pink |
| Hub Material | Polypropylene |
| Hub Type | Luer |
| Needle Gauge | 18 G |
| Needle Gauge (m) | 1.20 mm |
| Needle Length (in.) | 1-1/2 in. |
| Needle Length (m) | 38.10 mm |
| Needle Tip Type | BD Nokor |
| Needle Type | Fill |
| Needle Wall Type | Thin wall |
| Total Shelf Life | 1825 |
| Sterile | Sterilized product |
| Type Of Bevel | BD Nokor |
| Sterilization Method | Radiation |
| BPA Free | Not made with BPA |
| DEHP Free | Not made with DEHP |
| Latex Statement | Not made with natural rubber latex |
| PVC Free | Not made with PVC |
| Disposable | Disposable product |
| Single Use | Product is for single use only |
Regulatory Compliance and Quality System
BD Products comply with the regulatory requirements of the region in which these are sold and manufactured.
Sterility
All products which are labeled as #sterile# and released for sale by BD are certified to be sterile as long as the package is unopened and undamaged. For those products labeled #sterile fluid path#, only the fluid path is sterile. This product is primarily sterilized via Gamma radiation. Sterilization cycle development/validation is performed to 10-6 SAL in accordance with current ISO 11137 guidelines.
Biocompatability
This product has been evaluated in accordance with ISO 10993 “Biological Evaluation of Medical Devices”, and complies with all relevant sections.
Quality Control Testing and Release
Representative production samples are collected and inspected in accordance with current applicable product specifications. Inspection records are reviewed and signed off by qualified personnel for product release. The released devices meet applicable BD product specifications.
Device Characteristics
| What MRI safety information does the labeling contain? | Labeling does not contain MRI Safety Information |
| Device required to be labeled as containing natural rubber latex or dry natural rubber (21 CFR 801.437) | No |
| Device labeled as “Not made with natural rubber latex” | No |
| For Single-Use | Yes |
| Prescription Use (Rx) | Yes |
| Over the Counter (OTC) | No |
| Kit | No |
| Combination Product | No |
| Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P) | No |
Product Packaging Information
| Packaging Level | Shelfpack | Each | Case |
| Quantity | 100 | 1 | 1000 |
| Length | 116.0 mm | 451.0 mm | |
| Width | 88.0 mm | 206.0 mm | |
| Height | 98.0 mm | 129.0 mm | |
| Weight | 141.9 g | 1.419 g | 1.419 kg |
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