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BD 309593 - Safety-Lok Syringe LL 3cc 22gx1-1/2" 100/BX, 8 BX/CS
309593 - 3 mL BD Safety-Lok Syringe with needle attached 22 G x 1.5 in. Sterile, Single use
The BD Safety-Lok syringe offers clear visual and audible confirmation of the lock position.The only safety-engineered syringe of its type to offer clear visual confirmation of the lock position.
First In Safety,The worlds first safety-engineered syringe
Proven performance and dependability
- The only device of its kind to provide color-coded visual confirmation of the safety lock.
- Protective sleeve locks into position with one motion to cover the needle after injection.
- Crystal-clear barrel and sleeve allows for dosing visualization.
- Large flanges and tapered plunger rod increase control for easier aspiration and injection.
- Interim "park" position of safety shield complements injection practice in the OR.
- Can be used with any needle 1-1/2 in. or shorter - providing safety for many sizes that do not have other alternatives.
The BD Safety-Lok Syringe was designed for reliable performance
Key Product Features
Detachable Needle | Product has a detachable needle |
Hub Color | Black |
Hub Material | Polypropylene |
Hub Type | Luer |
Needle Gauge | 22 G |
Needle Gauge (m) | 0.70 mm |
Needle Length (in.) | 1 1/2 in. |
Needle Length (m) | 38.10mm |
Needle Tip Type | Regular |
Needle Type | Hypodermic |
Needle Wall Type | Regular |
Pyrogen Free | Product is pyrogen free |
Syringe Tip Orientation | Concentric |
Syringe Tip Type | BD Luer-Lok |
Syringe Scale | 0.1 ml graduations |
Total Shelf Life | 1825 |
Sterile | Sterilized product |
Volumetric Accuracy | +/- 5% *for 1ml or smaller,accuracy below 0.2ml is+/- 0.07ml |
Safety Engineered | Safety engineered product |
Safety Engineered Feature | Hypodermic syringe with sliding sleeve mechanism |
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.
Sterilization cycle development/validation is performed to 10-6 SAL in accordance with current ISO 11137 guidelines.
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.
Quick Reference Card
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 | 800 |
Length | 225.0 mm | 450.0 mm | |
Width | 185.0 mm | 375 | |
Height | 175.0 mm | 350 | |
Weight | 919.4 g | 9.194 g | 7.355 kg |