Curaplex
- Primary DI
- 00817617028989
- Brand
- Curaplex
- Company
- BOUND TREE MEDICAL, LLC
- Model
- 8600-01270
- Catalog number
- 8600-01270
- Device description
- *Custom* CCMC-Aerosol Nebulizer KIT (THS ONLY)
- 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 |
|---|
| 00817617028989 | Primary | GS1 | 0 | |
Alternate GTIN / UPC / EAN Codes
| Source identifier | GTIN-14 normalized | UPC-A | EAN-13 |
|---|
| 00817617028989 | 00817617028989 | 817617028989 | 0817617028989 |
GMDN Terms
| Term | Definition |
|---|
| Nebulizing system delivery set, single-use | A collection of flexible tubing, typically non-sterile, and associated items that may include a mask or mouthpiece, a medication chamber, and connectors, used with a nebulizer to deliver an aerosol, usually medicated, to the patient's respiratory system. It is made of synthetic material and is typically a thick-walled, anti-kink tubing to prevent blockage. 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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