HSW FINE-JECT®
- Primary DI
- 04035873048404
- Brand
- HSW FINE-JECT®
- Company
- Henke-Sass, Wolf GmbH
- Model
- 8300033531
- Catalog number
- 8300033531
- Device description
- HSW FINE-JECT®0,60X80MM / 23GX3 1/4" STERILE
- Published
- 2016-09-14
- 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 |
|---|
| 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 |
|---|
| 04035873048404 | Package | GS1 | 30 | In Commercial Distribution |
| 04035873048411 | Primary | GS1 | 0 | |
| 04035873052913 | Unit of Use | GS1 | 0 | |
Alternate GTIN / UPC / EAN Codes
| Source identifier | GTIN-14 normalized | EAN-13 |
|---|
| 04035873048404 | 04035873048404 | 4035873048404 |
| 04035873048411 | 04035873048411 | 4035873048411 |
| 04035873052913 | 04035873052913 | 4035873052913 |
GMDN Terms
| Term | Definition |
|---|
| Hypodermic needle, single-use | A non-dedicated, sharp bevel-edged, hollow tubular device intended to be inserted beneath the skin of a patient while connected to a noninvasive device (e.g., syringe, secondary medication set) to administer and/or withdraw (aspirate) fluids/drugs; it may also be used for fluid/drug preparation. Some types are designed with a shielding mechanism (e.g., safety cap) for protection from sharp injuries. It is not specifically designed for blood collection or artery puncture, and does not have wings for fixation/placement (i.e., not a blood collection, intra-arterial, or venous butterfly needle). This is a single-use device. |
Device Sizes
| Type | Value | Unit |
|---|
| Outer Diameter | 0.6 | Millimeter |
Storage And Handling
| Type | Low | High | Condition |
|---|
| Special Storage Condition, Specify | 0 | 0 | Keep dry |
Regulatory Flags
- DUNS number
- 317326411
- Device count
- 100
- DM exempt
- true
- 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
- true
- Sterilization required before use
- false
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