Arthrex®
- Primary DI
- 00888867042377
- Brand
- Arthrex®
- Company
- ARTHREX, INC.
- Model
- AR-8004-15S
- Catalog number
- AR-8004-15S
- Device description
- STAPLE, COMPRESSION, SS, 15I X 15L
- 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
Contact Domains#
Product Codes#
| Code | Name |
|---|---|
| HRS | Plate, fixation, bone |
Product Code Classifications#
| Code | Device | Specialty | Class |
|---|---|---|---|
| HRS | Plate, Fixation, Bone | Orthopedic | 2 |
Identifiers And Packaging#
| Identifier | Type | Agency | Package quantity | Status |
|---|---|---|---|---|
| 00888867042377 | Primary | GS1 | 0 | |
| M150AR800415S1 | Secondary | HIBCC | 0 |
Alternate GTIN / UPC / EAN Codes
| Source identifier | GTIN-14 normalized | UPC-A | EAN-13 |
|---|---|---|---|
| 00888867042377 | 00888867042377 | 888867042377 | 0888867042377 |
GMDN Terms#
| Term | Definition |
|---|---|
| Orthopaedic bone staple, non-adjustable | A non-bioabsorbable, implantable device designed to be inserted into fractured bone to achieve fixation and repair; the device may also be used to attach/secure structures (e.g., ligaments/tendons) to bone, or to reduce/cease bone growth in skeletal deformities (e.g., by being implanted across epiphysial cartilage). It is typically a curved or U-shaped device made of metal alloy material, and is not adjustable after it has been applied. Guides for drilling integrated into the handle of the staple and disposable devices associated with implantation may be included. |
Contacts#
| Phone | |
|---|---|
| +1(800)934-4404 | complaints@arthrex.com |
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
Other Devices From This Company#
| Primary DI | Brand | Model | Catalog | Published |
|---|---|---|---|---|
| 00888867007482 | Arthrex® | AR-13100-05.0S | AR-13100-05.0S | 2017-01-20 |
| 00888867007529 | Arthrex® | AR-13100-09.0S | AR-13100-09.0S | 2017-01-20 |
| 00888867007567 | Arthrex® | AR-13100-11.0S | AR-13100-11.0S | 2017-01-20 |
| 00888867007604 | Arthrex® | AR-13100-15.0S | AR-13100-15.0S | 2017-01-20 |
| 00888867007628 | Arthrex® | AR-13100-17.5S | AR-13100-17.5S | 2017-01-20 |
| 00888867008564 | Arthrex® | AR-13200-03.0S | AR-13200-03.0S | 2017-01-20 |
| 00888867204041 | Arthrex® | AR-8952XLS | AR-8952XLS | 2017-07-18 |
| 00888867210424 | Arthrex® | AR-8933L-26S | AR-8933L-26S | 2017-08-31 |
| 00888867210431 | Arthrex® | AR-8933L-28S | AR-8933L-28S | 2017-08-31 |
| 00888867210448 | Arthrex® | AR-8933L-30S | AR-8933L-30S | 2017-08-31 |
| 00888867210462 | Arthrex® | AR-8933L-34S | AR-8933L-34S | 2017-08-31 |
| 00888867210479 | Arthrex® | AR-8933L-36S | AR-8933L-36S | 2017-08-31 |
| 00888867210493 | Arthrex® | AR-8933L-40S | AR-8933L-40S | 2017-08-31 |
| 00888867251960 | Arthrex® | AR-8958-01S | AR-8958-01S | 2017-11-28 |
| 00888867266872 | Arthrex® | AR-8952PPL | AR-8952PPL | 2017-03-28 |
| 00888867266896 | Arthrex® | AR-8952PSR | AR-8952PSR | 2017-03-28 |
| 00888867266957 | Arthrex® | AR-8952PPR | AR-8952PPR | 2017-03-28 |
| 00888867371828 | Arthrex® | AR-8924S | AR-8924S | 2023-05-25 |
| 00888867251939 | Arthrex® | AR-8958-02 | AR-8958-02 | 2017-02-15 |
| 00888867279285 | Arthrex® | AR-7249-12-1 | AR-7249-12-1 | 2017-12-01 |
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