Arthrex®
- Primary DI
- 00888867183650
- Brand
- Arthrex®
- Company
- ARTHREX, INC.
- Model
- AR-9165-30NL
- Catalog number
- AR-9165-30NL
- Device description
- CENTRAL SCREW, NL, UNI REV, 6.5x30mm
- Published
- 2017-12-07
- Public version status
- Update
- Distribution status
- In Commercial Distribution
- MRI safety
- MR Conditional
- Rx
- true
- OTC
- false
- Sterile
- true
- Single use
- true
Contact Domains#
Product Codes#
| Code | Name |
|---|---|
| PHX | shoulder prosthesis, reverse configuration |
Product Code Classifications#
| Code | Device | Specialty | Class |
|---|---|---|---|
| PHX | Shoulder Prosthesis, Reverse Configuration | Orthopedic | 2 |
Identifiers And Packaging#
| Identifier | Type | Agency | Package quantity | Status |
|---|---|---|---|---|
| 00888867183650 | Primary | GS1 | 0 |
Alternate GTIN / UPC / EAN Codes
| Source identifier | GTIN-14 normalized | UPC-A | EAN-13 |
|---|---|---|---|
| 00888867183650 | 00888867183650 | 888867183650 | 0888867183650 |
GMDN Terms#
| Term | Definition |
|---|---|
| Shoulder glenoid fossa prosthesis, prefabricated | An implantable, prefabricated component of a total shoulder prosthesis (glenoid component) designed to replace or repair the glenoid fossa; it is not a custom-made device. It is cup-like in shape and typically made of polyethylene (PE), but may be made of metal or a combination of PE and metal; it may include fixation devices (e.g., screws) for attachment to the scapula. |
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 |
|---|---|---|---|---|
| 00888867020498 | Arthrex® | AR-1648 | AR-1648 | 2018-08-03 |
| 00888867319882 | Arthrex® | AR-8980BCT | AR-8980BCT | 2021-06-24 |
| 00888867501317 | Arthrex® | AR-1588SBR-RTT | AR-1588SBR-RTT | 2025-06-23 |
| 00888867328693 | Arthrex® | AR-8933VCL-10S | AR-8933VCL-10S | 2024-08-05 |
| 00888867328709 | Arthrex® | AR-8933VCL-12S | AR-8933VCL-12S | 2024-08-05 |
| 00888867328716 | Arthrex® | AR-8933VCL-14S | AR-8933VCL-14S | 2024-08-05 |
| 00888867328723 | Arthrex® | AR-8933VCL-16S | AR-8933VCL-16S | 2024-08-05 |
| 00888867328730 | Arthrex® | AR-8933VCL-18S | AR-8933VCL-18S | 2024-08-05 |
| 00888867328747 | Arthrex® | AR-8933VCL-20S | AR-8933VCL-20S | 2024-08-05 |
| 00888867328754 | Arthrex® | AR-8933VCL-22S | AR-8933VCL-22S | 2024-08-05 |
| 00888867328761 | Arthrex® | AR-8933VCL-24S | AR-8933VCL-24S | 2024-08-05 |
| 00888867328778 | Arthrex® | AR-8933VCL-26S | AR-8933VCL-26S | 2024-08-05 |
| 00888867328785 | Arthrex® | AR-8933VCL-28S | AR-8933VCL-28S | 2024-08-05 |
| 00888867328792 | Arthrex® | AR-8933VCL-30S | AR-8933VCL-30S | 2024-08-05 |
| 00888867328808 | Arthrex® | AR-8933VCL-32S | AR-8933VCL-32S | 2024-08-05 |
| 00888867328815 | Arthrex® | AR-8933VCL-34S | AR-8933VCL-34S | 2024-08-05 |
| 00888867328822 | Arthrex® | AR-8933VCL-36S | AR-8933VCL-36S | 2024-08-05 |
| 00888867328839 | Arthrex® | AR-8933VCL-38S | AR-8933VCL-38S | 2024-08-05 |
| 00888867328846 | Arthrex® | AR-8933VCL-40S | AR-8933VCL-40S | 2024-08-05 |
| 00888867328860 | Arthrex® | AR-8933HVCL-12S | AR-8933HVCL-12S | 2024-08-05 |
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|---|---|---|---|---|
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| 00840097513126 | Veritas Reverse Total Shoulder | Restor3d, Inc. | PHX | 2026-07-24 |
| 00840097513133 | Veritas Reverse Total Shoulder | Restor3d, Inc. | PHX | 2026-07-24 |
| 00840097516004 | Veritas Reverse Total Shoulder | Restor3d, Inc. | PHX | 2026-07-24 |
| 00840097516011 | Veritas Reverse Total Shoulder | Restor3d, Inc. | PHX | 2026-07-24 |
| 00811596031886 | Reverse Shoulder System | CATALYST ORTHOSCIENCE INC. | PHX | 2026-07-17 |
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