Description
Product Description
B Braun 4252500-02 - Introcan Safety IV Catheter 24 Ga. x 0.75 in., FEP, Straight, 200/CS
B Braun 4252500-02 Introcan Safety IV Catheter 24 Ga. x 0.75 in., FEP, Straight
Available sterile packaged. Contact representative for information on bulk, non-sterile options. Teflon is a registered trademark of E. I. du Pont de Nemours and Company.
- Teflon catheter material; straight hub
- Not Made With DEHP
- Not Made With Natural Rubber
- Not Made With PVC
B Braun 4252500-02 Introcan Safety IV Catheter Insertion Guide
Preparation
- Select and prepare site according to facility protocol.
- Completely remove the paper from the packaging.
- Remove protective cover by holding at each end, then pull straight apart.
- DO NOT ROTATE CATHETER PRIOR TO INSERTION
- Confirm catheter hub is seated tightly against flashback chamber.
Perform insertion
- Hold skin taut, insert catheter at optimal insertion angle.
- Visualize first flashback in flashback chamber to confirm needle entry in the vessel.
- Upon first flashback visualization, LOWER and advance the needle and catheter together approx 3mm or 1/8 in. to ensure catheter tip is in the vessel.
Thread catheter
- Holding needle still, advance the catheter off needle and visualize second flash within the catheter to confirm catheter is in the vessel.
- After confirmation, continue advancing catheter off the needle into the vessel.
- Release tourniquet.
Occlude vessel and stabilize catheter hub
Remove needle from catheter
- With hub stabilized, swiftly remove needle straight out from hub.
- The passive safety shield automatically covers the needle bevel.
- Properly discard needle into sharps container.
Connect and secure catheter
- Immediately CONNECT and TIGHTEN the accessory device to the catheter hub.
- Stabilize and dress the site per facility protocol.
Device Characteristics of B Braun 4252500-02 Introcan Safety IV Catheter 24 Ga. x 0.75 in., FEP, Straight
| 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": | Yes |
| 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 |