Identity
- Trade Name
- JETi Peripheral Catheter FDA UDI
- Generic Name
- Thrombectomy suction catheter FDA UDI
- Model / Reference
- WV6120-US FDA UDI
Identifiers
- Primary DI / UDI-DI
- B139WV6120US0 FDA UDI
- FDA Product Code
- DXE FDA UDI
- GMDN Term
- Thrombectomy suction catheter FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 870.5150 FDA UDI
- Commercial Distribution
- Not in Commercial Distribution FDA UDI
Clinical & Handling
Sterile
Yes
FDA UDI
Single Use
Yes
FDA UDI
Implantable
No
FDA UDI
Contains Latex
No
FDA UDI
Prescription Use
Yes
FDA UDI
Over-the-Counter
No
FDA UDI
Convenience Kit
No
FDA UDI
Combination Product
No
FDA UDI
HCT/P
No
FDA UDI
Premarket Exempt
No
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
Yes
FDA UDI
Ethylene Oxide FDA UDI
Dimensions & Sizes
- Size
- Length — 120 Centimeter FDA UDICatheter Gauge — 6 French FDA UDI
JETi Peripheral Catheter by Walk Vascular L.l.c. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Authorization Coverage (1 country)
Regulatory Authorizations
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class II | Pending data |
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Manufacturer
- Manufacturer
- Walk Vascular L.l.c.
Sources (1)
- FDA UDI e030a6e5-f349-47c3-adbc-9e6beafc2940 34 fields · synced Jun 6, 2026