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Part Number
Deroyal 6833
SKU Number
CIA8009180
Sell Unit
CASE
Ships Within
2-3 Days
List Price
$92.50
Product Description
Deroyal 6833 - Umbilical Cord Clamp, Sterile, 50/Bx, 2 Bxs/Cs
Deroyal 6833 Umbilical Cord Clamp Features and Benefits
- Snap-tight closure
- Will not loosen on tissue
- Clamp tested to over 11 lbs of pull-force
- Not made with natural rubber latex
Intended Use
The DeRoyal Umbilical Cord Clamp is intended to occlude the blood vessels in the umbilical cord of a newborn infant as the cord dries and shrinks after birth. The DeRoyal Umbilical Cord Clamp Cutter is intended to cut the umbilical cord clamp off the newborn.
Precautions
- This device is for single use only. It is not intended for disinfection and subsequent re-use, which may result in device failure or create the risk of contamination.
- This device has not been evaluated for reprocessing or re-sterilization. Reprocessing or re-sterilization may damage the device, rendering it unusable or may lead to device failure, which could result in patient illness, injury or death.
Directions for Use
- Visually examine the package for damage before opening. Replace clamp if the package or the device is damaged
- Open packaging using proper sterile technique.
- Visually inspect the clamp and clamp cutter for damage. Replace if device is damaged.
- Place the umbilical cord in the center of the clamp. Avoid placing the cord too close to the latch or hinge. Improper placement could result in injury to the patient.
- Press the cord clamp until it clicks, indicating the clamp is securely closed.
- Cut the umbilical cord in accordance with the current standard of care, but in no instance closer than inch (13 mm) from the clamp. Cutting too close to the clamp could cause the clamp to slip off the cord.
- Remove the cord clamp in accordance with the current standard of care.
- If necessary to remove, cut the clamp at the hinge area with the clamp cutter until completely severed
Deroyal 6833 Umbilical Cord Clamp 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" | 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 |