Arthrex®
- Primary DI
- 00888867336568
- Brand
- Arthrex®
- Company
- ARTHREX, INC.
- Model
- AR-1250S
- Catalog number
- AR-1250S
- Device description
- 2.4MM X 170MM DRILL TIP GUIDE PIN
- Published
- 2020-12-15
- Public version status
- Update
- Distribution status
- In Commercial Distribution
- MRI safety
- Labeling does not contain MRI Safety Information
- Rx
- true
- Sterile
- true
- Single use
- true
Contact Domains#
Product Codes#
| Code | Name |
|---|---|
| LXH | ORTHOPEDIC MANUAL SURGICAL INSTRUMENT |
Product Code Classifications#
| Code | Device | Specialty | Class |
|---|---|---|---|
| LXH | Orthopedic Manual Surgical Instrument | Orthopedic | 1 |
Identifiers And Packaging#
| Identifier | Type | Agency | Package quantity | Status |
|---|---|---|---|---|
| 00888867336568 | Primary | GS1 | 0 |
Alternate GTIN / UPC / EAN Codes
| Source identifier | GTIN-14 normalized | UPC-A | EAN-13 |
|---|---|---|---|
| 00888867336568 | 00888867336568 | 888867336568 | 0888867336568 |
GMDN Terms#
| Term | Definition |
|---|---|
| Cannulated surgical drill guiding pin | A sterile metal shaft (pin) designed to fit into the hollow centre of a cannulated surgical drill bit to provide a guide for drilling during a surgical procedure. The pin is bored into hard tissue (e.g., bone), typically by means of a surgical power tool handpiece, and the cannulated drill bit is subsequently fed over it during the drilling procedure. This is a single-use device. |
Sterilization Methods#
| Method |
|---|
Contacts#
| Phone | |
|---|---|
| +1(800)934-4404 | complaints@arthrex.com |
Regulatory Flags#
- DUNS number
- 131747628
- Device count
- 1
- Premarket exempt
- true
- Lot or batch
- true
- Expiration date on label
- true
Other Devices From This Company#
| Primary DI | Brand | Model | Catalog | Published |
|---|---|---|---|---|
| 00888867620964 | Arthrex® | AR-3210-0067 | AR-3210-0067 | 2026-10-12 |
| 00888867620971 | Arthrex® | AR-3210-0067-PK | AR-3210-0067-PK | 2026-10-12 |
| 00888867620988 | Arthrex® | AR-3210-0068 | AR-3210-0068 | 2026-10-12 |
| 00888867620995 | Arthrex® | AR-3210-0068-PK | AR-3210-0068-PK | 2026-10-12 |
| 00888867520745 | Arthrex® | AR-1360FT-KFT | AR-1360FT-KFT | 2026-01-21 |
| 00888867429857 | Arthrex® | AR-2600FSB-1 | AR-2600FSB-1 | 2023-05-24 |
| 00888867429864 | Arthrex® | AR-2600FSB-2 | AR-2600FSB-2 | 2023-05-24 |
| 00888867429871 | Arthrex® | AR-2600FSB-3 | AR-2600FSB-3 | 2023-05-24 |
| 00888867429888 | Arthrex® | AR-2600FSB-4 | AR-2600FSB-4 | 2023-05-24 |
| 00888867354067 | Arthrex® | AR-1360FT-BC | AR-1360FT-BC | 2020-12-15 |
| 00888867101951 | Arthrex® | AR-3600DC | AR-3600DC | 2018-12-21 |
| 00888867096066 | Arthrex® | AR-1677BC-CP | AR-1677BC-CP | 2017-02-15 |
| 00888867084384 | Arthrex® | ABS-3005 | ABS-3005 | 2017-02-15 |
| 00888867084407 | Arthrex® | ABS-3008 | ABS-3008 | 2017-02-15 |
| 00888867084421 | Arthrex® | ABS-3016 | ABS-3016 | 2017-02-15 |
| 00888867084148 | Arthrex® | ABS-2001-01 | ABS-2001-01 | 2017-02-15 |
| 00888867084155 | Arthrex® | ABS-2001-02 | ABS-2001-02 | 2017-02-15 |
| 00888867084162 | Arthrex® | ABS-2001-05 | ABS-2001-05 | 2017-02-15 |
| 00888867084179 | Arthrex® | ABS-2001-10 | ABS-2001-10 | 2017-02-15 |
| 00888867084186 | Arthrex® | ABS-2002-01 | ABS-2002-01 | 2017-02-15 |
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|---|---|---|---|---|
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| 00850080243176 | OSTEOROD Delivery System | BONE SOLUTIONS, INC. | LXH | 2026-10-12 |
| 00889795150264 | APEX 3D Total Ankle Replacement System | Paragon 28, Inc. | LXH | 2026-10-12 |
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