ARROW
- Primary DI
- 30801902170324
- Brand
- ARROW
- Company
- TELEFLEX INCORPORATED
- Model
- IPN917316
- Catalog number
- 9001-VC-001
- Device description
- EZ-IO(R) 25mm Needle Set
- Published
- 2020-10-19
- Public version status
- New
- Distribution status
- In Commercial Distribution
- MRI safety
- MR Unsafe
- Rx
- true
- OTC
- false
- Sterile
- true
- Single use
- true
Product Codes
| Code | Name |
|---|
| FMI | Needle, hypodermic, single lumen |
Product Code Classifications
| Code | Device | Specialty | Class |
|---|
| FMI | Needle, Hypodermic, Single Lumen | General Hospital | 2 |
Identifiers And Packaging
| Identifier | Type | Agency | Package quantity | Status |
|---|
| 20801902170327 | Package | GS1 | 1 | In Commercial Distribution |
| 30801902170324 | Package | GS1 | 50 | In Commercial Distribution |
| 10801902170320 | Primary | GS1 | 0 | |
Alternate GTIN / UPC / EAN Codes
| Source identifier | GTIN-14 normalized |
|---|
| 20801902170327 | 20801902170327 |
| 30801902170324 | 30801902170324 |
| 10801902170320 | 10801902170320 |
GMDN Terms
| Term | Definition |
|---|
| Intraosseous infusion kit | A collection of sterile devices designed to perform an intraosseous (IO) infusion (i.e., an infusion directly into the bone's medullary cavity for the purpose of administering emergency medications and other fluids). It typically consists of a needle (possibly of a special design), an inserting handle, a scalpel, an infusion set, swabs and sutures. This device is used as an alternate to the preferred intravenous (IV) route when this cannot be established in a timely manner, typically during cardiac arrest, patients with respiratory failure or in shock, and when peripheral IV infusion is very difficult. This is a single-use device. |
Regulatory Flags
- DUNS number
- 002348191
- 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
- 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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