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Product Description
GE Healthcare Part #002200 - CUFF, INFANT, 2-TUBE SUB-MINI, RUST, 5/BX
GE Critikon DURA-CUF Blood Pressure Cuffs
Dura-Cuf Blood Pressure Cuffs, Dual-Tube, Submin Connector For GE Eagle, Dash, Tram, Solar, MAC-Lab Systems
The first GE CRITIKON blood pressure cuff, the DURA-CUF is gentle, yet designed for durability. Made with tough, flexible nylon, they are convenient and easy to clean with curved corners to enhance your patients comfort. The DURA-CUF is constructed for multiple patient use in low acuity care settings. They are also ideal for the physician office where the risk of contamination is diminished.
| Product Code | Ref. No. | Size | Color | Limb Circumference | Connector |
| 002200 | E2200J | Infant | Orange | 8 - 13cm | 2-Tube Submin Connector |
Our DURA-CUF BP cuff line is gentle and comfortable, yet designed for durability
- Gentle nylon, strong enough for repeated inflation
- Reusable for multiple patient use
- Convenient and easy to clean
- Color-coded by size for accuracy and added patient comfort
- Sized to meet AHA, AAMI/ANSI/SP9 and EN1060 requirements
- Easy-to-use range markers and index line for proper size and placement
- Extra hook and loop for added security
- Variety of connection types to fit multiple monitoring systems
- Latex-free, PVC-free
Designed for patient safety, comfort and accuracy
- Made with durable materials that can withstand extensive use and multiple disinfections and cleanings
- Designed with rounded corners to enhance patient comfort
- Constructed with materials not made with PVC, making them safer for the environment, and natural rubber latex, making them safer for your patient
- Compliant with AAMI and AHA NIBP cuff sizing standards for prompt, correct sizing
Suitable for virtually every physicians office
- Full range of adapters and connectors are compatible with automated monitors from GE, Philips**, Spacelabs**, and Datascope**, as well as on a variety of manual devices, including wall manometers and hand-held gauges
- Three types of cuff assortment packs enable for easier ordering and optimizing inventory space
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): | Yes |
| 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 |