FDA UDI
Not in Commercial Distribution
🇺🇸 United States
JETi Peripheral Catheter
DI: B139WV81000
·
Model: WV8100
·
WALK VASCULAR L.L.C.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1
Basic Information
- Brand Name
- JETi Peripheral Catheter
- Primary DI
- B139WV81000
- Version / Model
- WV8100
- Catalog Number
- WV8100
- Company Name
- WALK VASCULAR L.L.C.
- Labeler DUNS
- 034774488
- Distribution Status
- Not in Commercial Distribution
- Device Count in Pkg
- 1
- Record Status
- Published
- Publish Date
- 2017-08-21
- Public Version
- 7
- Public Version Date
- 2022-11-09
- Public Version Status
- Update
- Public Device Record Key
- f8cb0569-417d-483d-b614-ae794f281b8e
- Distribution End Date
- 2018-08-08
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 |
|---|---|---|---|---|
| DXE | Catheter, Embolectomy | Cardiovascular | 870.5150 | 2 |
GMDN Terms
| Code | Name | Definition | Implantable | Status |
|---|---|---|---|---|
| 58173 | Thrombectomy suction catheter | A flexible or semi-flexible tube designed for the percutaneous, transluminal disruption and removal of clotted blood (i.e., a thrombus or thromboembolus) or other formed elements causing vascular obstruction in native/stented blood vessels, native/synthetic bypass grafts, and/or haemodialysis access grafts, through suction (aspiration) in conjunction with a syringe or dedicated suction pump system (pump not included). It may additionally be intended for infusion of fluids and/or used as a guide-catheter to facilitate introduction of a thrombectomy wire-net (not included) to remove residual thrombus. Collection containers may be included with the catheter. This is a single-use device. | No | Active |
Identifiers
| Type | ID | Issuing Agency | Package Type | Qty per Pkg | Pkg Status | Pkg Discontinue Date |
|---|---|---|---|---|---|---|
| Primary | B139WV81000 | HIBCC | ||||
| Package | B139WV81001 | HIBCC | Carton Box | 1 | Not in Commercial Distribution | 2018-08-08 |
Device Sizes
| Type | Value | Unit | Text |
|---|---|---|---|
| Length | 100 | Centimeter | |
| Catheter Gauge | 8 | French |