Arthrex®
- Primary DI
- 00888867319950
- Brand
- Arthrex®
- Company
- ARTHREX, INC.
- Model
- ABS-2016-03
- Catalog number
- ABS-2016-03
- Device description
- BioSurge Kit w/ 15mmx40mmx3mm
- Published
- 2019-05-20
- 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 |
|---|---|
| ORG | Platelet and plasma separator for bone graft handling |
Product Code Classifications#
| Code | Device | Specialty | Class |
|---|---|---|---|
| ORG | Platelet And Plasma Separator For Bone Graft Handling | Hematology | 2 |
Identifiers And Packaging#
| Identifier | Type | Agency | Package quantity | Status |
|---|---|---|---|---|
| 00888867319950 | Primary | GS1 | 0 |
Alternate GTIN / UPC / EAN Codes
| Source identifier | GTIN-14 normalized | UPC-A | EAN-13 |
|---|---|---|---|
| 00888867319950 | 00888867319950 | 888867319950 | 0888867319950 |
GMDN Terms#
| Term | Definition |
|---|---|
| Haematological concentrate system preparation kit, platelet concentration | A collection of devices designed to prepare platelet-rich plasma (PRP) or platelet-rich fibrin matrix (PRFM) from an autologous blood specimen for application to soft-tissue wounds and injured bone to accelerate healing and/or achieve haemostasis. It includes single- or double- (concentric) barrel syringe(s) with connecting tubes and caps. Blood is collected by venous puncture and processed in a centrifuge, increasing the concentration of platelets within the plasma or fibrin matrix; this may be done at the point-of-care. This is a single-use device. |
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
- true
- Combination product
- true
- Lot or batch
- true
- Serial number
- true
- 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 |
|---|---|---|---|---|
| 00888867576032 | Arthrex® | AR-3636-REMP | AR-3636-REMP | 2026-10-20 |
| 00888867576056 | Arthrex® | AR-3641SP-REMP | AR-3641SP-REMP | 2026-10-20 |
| 00888867576070 | Arthrex® | AR-6573-1 | AR-6573-1 | 2026-10-20 |
| 00888867576087 | Arthrex® | AR-6573-2 | AR-6573-2 | 2026-10-20 |
| 00888867568280 | Arthrex® | AR-3210-0050-SJ | AR-3210-0050-SJ | 2026-10-16 |
| 00888867568297 | Arthrex® | AR-3210-0051-SJ | AR-3210-0051-SJ | 2026-10-16 |
| 00888867568303 | Arthrex® | AR-3210-0059-PK | AR-3210-0059-PK | 2026-10-16 |
| 00888867568310 | Arthrex® | AR-3210-0063-PK | AR-3210-0063-PK | 2026-10-16 |
| 00888867568457 | Arthrex® | AR-8650DS-N | AR-8650DS-N | 2026-10-16 |
| 00888867427143 | Arthrex® | AR-S6524-025-230C | AR-S6524-025-230C | 2023-06-05 |
| 00888867389533 | Arthrex® | AR-9928BCK-MIS | AR-9928BCK-MIS | 2023-05-22 |
| 00888867276086 | Arthrex® | AR-9437-16 | AR-9437-16 | 2022-07-15 |
| 00888867060401 | Arthrex® | AR-9439-16 | AR-9439-16 | 2018-06-02 |
| 00888867060418 | Arthrex® | AR-9439-18 | AR-9439-18 | 2018-06-02 |
| 00888867060425 | Arthrex® | AR-9441-16 | AR-9441-16 | 2018-06-14 |
| 00888867060432 | Arthrex® | AR-9441-18 | AR-9441-18 | 2018-06-02 |
| 00888867060449 | Arthrex® | AR-9443-16 | AR-9443-16 | 2018-06-14 |
| 00888867060456 | Arthrex® | AR-9443-18 | AR-9443-18 | 2018-06-14 |
| 00888867060463 | Arthrex® | AR-9445-17 | AR-9445-17 | 2018-06-28 |
| 00888867060470 | Arthrex® | AR-9445-19 | AR-9445-19 | 2018-06-02 |
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