Curaplex
- Primary DI
- 00817617028866
- Brand
- Curaplex
- Company
- BOUND TREE MEDICAL, LLC
- Model
- 301-8600-01266
- Catalog number
- 301-8600-01266
- Device description
- *Custom* Curaplex Aerosol Nebulizer Kit
- Published
- 2017-12-12
- Public version status
- Update
- Distribution status
- In Commercial Distribution
- MRI safety
- Labeling does not contain MRI Safety Information
- Rx
- true
- OTC
- false
- Sterile
- false
- Single use
- true
Product Codes
| Code | Name |
|---|
| CAF | NEBULIZER (DIRECT PATIENT INTERFACE) |
Product Code Classifications
| Code | Device | Specialty | Class |
|---|
| CAF | Nebulizer (Direct Patient Interface) | Anesthesiology | 2 |
Identifiers And Packaging
| Identifier | Type | Agency | Package quantity | Status |
|---|
| 00817617028866 | Primary | GS1 | 0 | |
Alternate GTIN / UPC / EAN Codes
| Source identifier | GTIN-14 normalized | UPC-A | EAN-13 |
|---|
| 00817617028866 | 00817617028866 | 817617028866 | 0817617028866 |
GMDN Terms
| Term | Definition |
|---|
| Nebulizing adaptor | A small connecting device, which includes an integrated nebulizer, intended to join a sterile water or sterile isotonic sodium chloride solution reservoir to a respiratory gas source (typically wall outlet) and a gas administration device (e.g., mask, mouthpiece). It is designed to generate aerosolized fluid (finely dispersed airborne droplets in a liquid phase) to be inhaled by a patient with a respiratory disorder [e.g., chronic obstructive pulmonary disease (COPD), cystic fibrosis (CF)]. This is a single-use device. |
Regulatory Flags
- DUNS number
- 070556204
- Device count
- 1
- DM exempt
- true
- Premarket exempt
- true
- HCT/P
- false
- Kit
- true
- Combination product
- false
- Lot or batch
- true
- Serial number
- false
- Manufacturing date on label
- false
- Expiration date on label
- true
- Donation ID number
- false
- Contains natural rubber latex
- false
- No natural rubber latex
- false
- Sterilization required before use
- false
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