FDA UDI
In Commercial Distribution
🇺🇸 United States
Diamondback Peripheral
DI: 10850000491189
·
Model: DBP-125SOLID145
·
Cardiovascular Systems, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1
Basic Information
- Brand Name
- Diamondback Peripheral
- Primary DI
- 10850000491189
- Version / Model
- DBP-125SOLID145
- Catalog Number
- 7-10057-02
- Company Name
- Cardiovascular Systems, Inc.
- Labeler DUNS
- 024954518
- Distribution Status
- In Commercial Distribution
- Device Count in Pkg
- 1
- Record Status
- Published
- Publish Date
- 2019-11-13
- Public Version
- 1
- Public Version Date
- 2019-11-21
- Public Version Status
- New
- Public Device Record Key
- e02d4b0c-a701-4739-b473-45e113cd1f2f
Device Description
DIAMONDBACK PERIPHERAL, SOLID CROWN, 1.25MM, 145CM SHAFT
Device Characteristics
- Single Use
- Yes
- Prescription Use (Rx)
- Yes
- Over the Counter (OTC)
- No
- Kit
- No
- Combination Product
- No
- HCT/P
- No
- Contains NRL
- No
- Not Made with NRL
- No
- MRI Safety
- Labeling does not contain MRI Safety Information
- Direct Marking Exempt
- No
- PM Exempt
- No
- Has Serial Number
- No
- Has Lot/Batch Number
- Yes
- Has Manufacturing Date
- No
- Has Expiration Date
- Yes
- Has Donation ID
- No
Sterilization
- Is Sterile
- Yes
- Sterilization Prior Use
- Yes
- Sterilization Methods
- Ethylene Oxide
Product Codes
| Code | Name | Medical Specialty | Regulation # | Device Class |
|---|---|---|---|---|
| MCW | Catheter, Peripheral, Atherectomy | Cardiovascular | 870.4875 | 2 |
GMDN Terms
| Code | Name | Definition | Implantable | Status |
|---|---|---|---|---|
| 44307 | Mechanical atherectomy system catheter, peripheral | A sterile, flexible tube (catheter) intended to be percutaneously introduced for the intraluminal mechanical disruption of atheroma plaque from the walls of peripheral arteries. It has a power-driven cutting or abrasive head for slicing/grinding the atheroma into fragments small enough to be aspirated or absorbed. This device is not intended for use in the coronary, carotid, iliac or renal vasculature. This is a single-use device. | No | Active |
Identifiers
| Type | ID | Issuing Agency | Package Type | Qty per Pkg | Pkg Status | Pkg Discontinue Date |
|---|---|---|---|---|---|---|
| Primary | 10850000491189 | GS1 |
Customer Contacts
- Phone
- 877-274-0360
- [email protected]
- Phone
- 651-259-1600
- [email protected]
Device Sizes
| Type | Value | Unit | Text |
|---|---|---|---|
| Device Size Text, specify | Intro Sheath: 4 Fr | ||
| Device Size Text, specify | Max OD: 0.052 inches | ||
| Device Size Text, specify | Crown Type: Solid | ||
| Device Size Text, specify | high speed: 120 krpm | ||
| Device Size Text, specify | medium speed: 90 krpm | ||
| Device Size Text, specify | low speed: 60 krpm | ||
| Device Size Text, specify | guidewire size OD: 0.014 inches | ||
| Device Size Text, specify | shaft length: 145 cm | ||
| Device Size Text, specify | nose length: 7 mm | ||
| Device Size Text, specify | Crown diameter: 1.25 mm |