Identity
- Trade Name
- AXS VECTA 46 FDA UDI
- Generic Name
- Thrombectomy suction catheter FDA UDI
- Device Name
- Intermediate Catheter FDA UDI
- Model / Reference
- INC-11814-146 FDA UDI
- Description
- Intermediate Catheter FDA UDI
Identifiers
- Catalog Number
- INC-11814-146 FDA UDI
- Primary DI / UDI-DI
- 07613327519365 FDA UDI
- FDA Product Code
- QJP FDA UDINRY FDA UDI
- GMDN Term
- Thrombectomy suction catheter FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 870.1250 FDA UDI
- Commercial Distribution
- 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
No
FDA UDI
Dimensions & Sizes
- Size
- Lumen/Inner Diameter — 0.046 Inch FDA UDILength — 146.0 Centimeter FDA UDI
Category: Vascular guide-catheter, single-useThrombectomy suction catheter
Axs Vecta 46 by Stryker Corp. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Thrombectomy suction catheter.
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- Indigo System — PENUMBRA, INC. · Class II
- Penumbra System — PENUMBRA, INC. · Class II
- Penumbra System — PENUMBRA, INC. · Class II
- Pounce ™ Thrombectomy — Surmodics, Inc. · Class II
- Solitaire™ — Micro Therapeutics, Inc. · Class II
Cleared under the same submission
K190338 also covers:
K202752 also covers:
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
- Stryker Corp.
Sources (1)
- FDA UDI e4438ca1-2bd8-4f3a-bb27-150eb770cff7 38 fields · synced May 30, 2026