Product Description
Welch-Allyn 1903XLDX – CUFF, OMNI, XL / ADULT, 2TUBE, MATED, SUBMINI, C, EACH
Welch Allyn Trimline Blood Pressure Cuff; Size-11L Adult Long, Reusable, 2-Tubes (10.0 in/25.4 cm), Mated Subminiature (#5082-182 and #5082-178) Connectors
Trimline technology offers a proven, dependable reusable cuff solution you know and trust. Using traditional tube-and-connector configurations, facilities that standardize on Trimline will have minimal impact on nursing workflow with this reliable cuff solution.
Features
- Traditional multi-use reusable cuff that can be cleaned between uses
- Full range of sizes available, meets all applicable AAMI standards
- Exterior Range guide and BALANCED Bladder to help ensure accurate readings
- Two-year warranty
Item Specifications
- Part Number:1903XLDX
- GTIN:00732094015805
- Warranty: TWO YEAR WARRANTY
A Traditional Style Blood Pressure Cuff with Enhanced Design to Facilitate Accurate Readings
- Color coding helps clinicians quickly identify the proper size cuff
- Completely latex-free with antimicrobial agents applied to help prevent bacterial growth and mildew on the cuff fabric
- Connects to all manual and NIBP monitors
- Exterior Pre-Gaged range guide and BALANCED bladder design help to ensure accurate readings by faciliating proper arterial compression.
- Trimline Reusable blood pressure cuffs are made out of Nylon.
How Can Trimline Help You?
Environmental Specifications
NOTE: Comply with regional law when non-automated sphygmomanometer or accessories are discarded.
| Storage temperature | -20 ℃ to 70 ℃ (-4 ℉ to 158 ℉) |
| Storage relative humidity | 15% to 95% (noncondensing) |
| Operating temperature | 10 ℃ to 40 ℃ (50 ℉ to 104 ℉) |
| Operating relative humidity | 15% to 90% (noncondensing) |
Shipping Weights and Dimensions
| Gross Weight: | 0.07 KG |
| Width: | 22.86 CM |
| Height: | 27.94 CM |
| Depth: | 2.54 CM |
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: | No |
| 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 |
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