Curaplex
- Primary DI
- 00817617021850
- Brand
- Curaplex
- Company
- BOUND TREE MEDICAL, LLC
- Model
- 533-MS-25058EA
- Device description
- Curaplex Oxygen Mask, Pediatric, Elongated, Total NRB, w/o Safety vent, 7 ft Tubing 50ea/cs
- Published
- 2017-02-06
- Public version status
- Update
- Distribution status
- In Commercial Distribution
- MRI safety
- Labeling does not contain MRI Safety Information
- Rx
- true
- OTC
- false
- Sterile
- true
- Single use
- true
Product Code Classifications
| Code | Device | Specialty | Class |
|---|
| BYG | Mask, Oxygen | Anesthesiology | 1 |
Identifiers And Packaging
| Identifier | Type | Agency | Package quantity | Status |
|---|
| 00817617021850 | Package | GS1 | 50 | In Commercial Distribution |
| 00817617022758 | Primary | GS1 | 0 | |
Alternate GTIN / UPC / EAN Codes
| Source identifier | GTIN-14 normalized | UPC-A | EAN-13 |
|---|
| 00817617021850 | 00817617021850 | 817617021850 | 0817617021850 |
| 00817617022758 | 00817617022758 | 817617022758 | 0817617022758 |
GMDN Terms
| Term | Definition |
|---|
| Foetal scalp electrode, spiral | A sterile electrical conductor designed to transmit electric signals from the foetal scalp to an intrapartum monitor. The device is a spiralled (either single- or double-helix) metallic electrode with a sharp tip that is directly inserted into the foetal scalp with a screwing action; and an adaptor cable that may include a transducer. The electrode penetrates into the scalp up to 2.5 mm (0.1 inch); it is usually inserted with a dedicated applicator that may be included. The electrode is typically used to monitor a foetal physiologic signal (e.g., heart rate) during labour (intrapartum) after rupture of the amniotic sac. This is a single-use device. |
Regulatory Flags
- DUNS number
- 070556204
- Device count
- 1
- DM exempt
- false
- Premarket exempt
- true
- HCT/P
- false
- Kit
- false
- Combination product
- false
- Lot or batch
- true
- Serial number
- false
- Manufacturing date on label
- true
- Expiration date on label
- true
- Donation ID number
- false
- Contains natural rubber latex
- false
- No natural rubber latex
- true
- Sterilization required before use
- true
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