Arthrex®
- Primary DI
- 00888867102453
- Brand
- Arthrex®
- Company
- ARTHREX, INC.
- Model
- AR-4155P-2500
- Catalog number
- AR-4155P-2500
- Device description
- 3 X 25MM PIP DART, PEEK, STRAIGHT
- Published
- 2017-02-15
- 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 |
|---|
| HTY | PIN, FIXATION, SMOOTH |
Product Code Classifications
| Code | Device | Specialty | Class |
|---|
| HTY | Pin, Fixation, Smooth | Orthopedic | 2 |
Identifiers And Packaging
| Identifier | Type | Agency | Package quantity | Status |
|---|
| 00888867102453 | Primary | GS1 | 0 | |
| M150AR4155P25001 | Secondary | HIBCC | 0 | |
Alternate GTIN / UPC / EAN Codes
| Source identifier | GTIN-14 normalized | UPC-A | EAN-13 |
|---|
| 00888867102453 | 00888867102453 | 888867102453 | 0888867102453 |
GMDN Terms
| Term | Definition |
|---|
| Tendon/ligament bone anchor, non-bioabsorbable | A non-bioabsorbable device designed to be implanted into bone for the attachment of tendons/ligaments/soft tissues either directly or via a suture attached to the device; typically used in arthroscopic or open surgical procedures. This device is available in various designs and sizes and is made of a material that cannot be chemically degraded or absorbed via natural body processes [e.g., titanium (Ti)]. |
Regulatory Flags
- DUNS number
- 131747628
- 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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