HARVEST®
- Primary DI
- 05020583514485
- Brand
- HARVEST®
- Company
- TERUMO BCT, INC.
- Model
- 51448
- Device description
- BAN-25 8Ga BM Aspirate Needle
- Published
- 2017-07-15
- Public version status
- Update
- Distribution status
- Not 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 |
|---|---|
| FMF | Syringe, piston |
Product Code Classifications#
| Code | Device | Specialty | Class |
|---|---|---|---|
| FMF | Syringe, Piston | General Hospital | 2 |
Premarket Submissions#
| Submission | Supplement |
|---|---|
| K103340 | 000 |
Premarket Details#
Identifiers And Packaging#
| Identifier | Type | Agency | Package quantity | Status |
|---|---|---|---|---|
| 35020583514486 | Package | GS1 | 3 | In Commercial Distribution |
| 05020583514485 | Primary | GS1 | 0 |
Alternate GTIN / UPC / EAN Codes
| Source identifier | GTIN-14 normalized | EAN-13 |
|---|---|---|
| 35020583514486 | 35020583514486 | |
| 05020583514485 | 05020583514485 | 5020583514485 |
GMDN Terms#
| Term | Definition |
|---|---|
| Bone graft delivery kit | A collection of sterile devices intended to be used to prepare and/or deliver bone graft material during an orthopaedic surgical procedure. It typically includes aspirating/delivery/mixing syringe(s), an adaptor, and a needle/cannula. It allows for the aspiration and/or premixing of bone marrow, autologous blood, plasma, intravenous fluids (IVF), and bone void filler (e.g., allograft, autograft, synthetic bone graft material), and their delivery to the surgical site. This is a single-use device. |
Storage And Handling#
| Type | Low | High | Condition |
|---|---|---|---|
| Storage Environment Temperature | 0 Degrees Celsius | 25 Degrees Celsius |
Sterilization Methods#
| Method |
|---|
Contacts#
| Phone | |
|---|---|
| +1(877)339-4228 | FDAUDIprogram@terumobct.com |
Regulatory Flags#
- DUNS number
- 801679200
- Device count
- 1
- Kit
- true
- Lot or batch
- true
- Expiration date on label
- true
- No natural rubber latex
- true
Other Devices From This Company#
| Primary DI | Brand | Model | Catalog | Published |
|---|---|---|---|---|
| 05020583103108 | Spectra Optia® | 10310 | 2016-09-15 | |
| 05020583610002 | Spectra Optia® | 61000 | 2016-09-15 | |
| 05020583001145 | Reveos® Automated Whole Blood Processing System | 24000 | 2025-08-06 | |
| 05020583826502 | Trima Accel | 82650 | 2023-06-19 | |
| 05020583803664 | Trima Accel® | 80366 | 2017-02-15 | |
| 05020583804005 | Trima Accel® | 80400 | 2016-09-15 | |
| 05020583824089 | Trima Accel® | 82408 | 2016-09-15 | |
| 05020583826601 | Trima Accel® | 82660 | 2016-09-15 | |
| 05020583826663 | Trima Accel® | 82666 | 2017-02-15 | |
| 05020583700512 | Blood Component Sampling Sets | 70051 | 2016-09-15 | |
| 05020583803565 | Trima Accel® | 80356 | 2017-02-15 | |
| 05020583804401 | Trima Accel® | 80440 | 2016-09-15 | |
| 05020583824409 | Trima Accel® | 82440 | 2016-09-15 | |
| 05020583803503 | Trima Accel® | 80350 | 2016-09-15 | |
| 05020583803701 | Trima Accel® | 80370 | 2016-09-15 | |
| 05020583803404 | Trima Accel® | 80340 | 2016-09-15 | |
| 05020583803602 | Trima Accel® | 80360 | 2016-09-15 | |
| 05020583807006 | Trima Accel® | 80700 | 2016-09-15 | |
| 05020583804500 | Trima Accel® | 80450 | 2016-09-15 | |
| 05020583805002 | Trima Accel® | 80500 | 2016-09-15 |
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| 05391530754255 | polycarbonate syringe | DMC MEDICAL LIMITED | FMF | 2026-09-27 |
| 05391530754279 | polycarbonate syringe | DMC MEDICAL LIMITED | FMF | 2026-09-27 |
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| 05391530754323 | polycarbonate syringe | DMC MEDICAL LIMITED | FMF | 2026-09-27 |
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| 05391530754415 | polycarbonate syringe | DMC MEDICAL LIMITED | FMF | 2026-09-27 |
| 05391530754477 | polycarbonate syringe | DMC MEDICAL LIMITED | FMF | 2026-09-27 |
| 05391530754484 | polycarbonate syringe | DMC MEDICAL LIMITED | FMF | 2026-09-27 |
| 05391530754651 | polycarbonate syringes | DMC MEDICAL LIMITED | FMF | 2026-09-27 |
| 05391530754736 | polycarbonate syringe | DMC MEDICAL LIMITED | FMF | 2026-09-27 |
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