Deroyal M8139 – Single Strap Security Cuff, Tri-Clip Buckle, 1/Pair
Deroyal M8139 Single Strap Security Cuff
- Neoprene construction that may be easily cleaned for hygiene purposes
- Double hook and loop wrist closure provides durability and maximum security
- Additional quick-release (QR) buckle around wrist closure for more security (M8138 only)
- Strap attaches with hook and loop or quick-release (QR) buckle
- Cuffs can be trimmed to ensure best fit
- Pediatric size available (M8139-P)
Deroyal M8139 Single Strap Security Cuff Specifications
Catalog No. | Cuff Closure | Strap Attachment |
M8139 | Tri-Clip Buckle | Tri-Clip Buckle |
Cuff Dimensions | Strap Length | QTY |
14″ L x 3″ W | 49″ | 1/Pair |
Deroyal M8139 Single Strap Security Cuff Indications
Highly agitated and/or violent patients at risk of injuring themselves and/or others
Deroyal M8139 Single Strap Security Cuff Intended Use
The DeRoyal Double-Strap Security Cuffs are intended to be prescribed by a properly licensed practitioner to protect the patient from harming themselves, other patients, family members and/or staff.
Contraindications of Deroyal M8139 Single Strap Security Cuff
Never use on a patient if an I.V. or wound site could be compromised by the device.
Deroyal M8139 Single Strap Security Cuff Instructions for Use
- Secure the cuffs to the bed or gurney. Release the female end of the buckle and wrap its strap around the anchor.
- Pull the female portion through the loop and connect the male and female ends of the buckle.
- Pull the excess strap to tighten. NOTE: Secure excess strap from patients reach.
- Once all security cuffs are applied to the bed or gurney, secure the cuffs on the patient.
- Wrap the neoprene cuff around the patients wrist or ankle with the loose neoprene side first and then follow with the neoprene side with hook. Secure the loop side of the cuff and follow with the other hook side of the cuff.
Device Characteristics of Deroyal M8139 Single Strap Security Cuff
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 |