FDA UDI
In Commercial Distribution
🇺🇸 United States
Diamondback Peripheral
DI: 10852528005244
·
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
- 10852528005244
- Version / Model
- DBP-125SOLID145
- Catalog Number
- DBP-125SOLID145
- Company Name
- Cardiovascular Systems, Inc.
- Labeler DUNS
- 024954518
- Distribution Status
- In Commercial Distribution
- Device Count in Pkg
- 1
- Record Status
- Published
- Publish Date
- 2015-12-04
- Public Version
- 3
- Public Version Date
- 2018-04-17
- Public Version Status
- Update
- Public Device Record Key
- 6ae2af66-0918-405d-b386-d5a41e96118e
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 | 10852528005244 | GS1 |
Customer Contacts
- Phone
- 651-259-1600
- [email protected]
Device Sizes
| Type | Value | Unit | Text |
|---|---|---|---|
| Device Size Text, specify | Crown Type, Solid | ||
| Device Size Text, specify | Intro Sheath 4 Fr | ||
| Device Size Text, specify | Max OD 0.052 inches | ||
| 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 |