Curaplex
- Primary DI
- 00817617023922
- Brand
- Curaplex
- Company
- BOUND TREE MEDICAL, LLC
- Model
- 10-83011NEG
- Catalog number
- 10-83011NEG
- Device description
- Curaplex IV Admin Set, 10 Drop, 83 in, 1 LL Site, 1 PP Site, Spin Lock Connection
- Published
- 2017-04-18
- 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 Codes
| Code | Name |
|---|
| LHI | Set, i.V. Fluid transfer |
Product Code Classifications
| Code | Device | Specialty | Class |
|---|
| LHI | Set, I.V. Fluid Transfer | General Hospital | 2 |
Identifiers And Packaging
| Identifier | Type | Agency | Package quantity | Status |
|---|
| 00817617023922 | Package | GS1 | 50 | In Commercial Distribution |
| 00817617023861 | Primary | GS1 | 0 | |
GMDN Terms
| Term | Definition |
|---|
| Intravenous administration tubing extension set | A collection of tubing and connectors intended to establish an extension of tubing where the standard length of the tubing in an intravenous (IV) administration set is insufficient. This is a single-use device. |
Regulatory Flags
- DUNS number
- 070556204
- Device count
- 1
- DM exempt
- false
- Premarket exempt
- false
- 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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