Axs Vecta 46

FDA UDI

Class II (US FDA UDI)

by Stryker Corp.

Identity

Trade Name: AXS VECTA 46 FDA UDI
Generic Name: Vascular guide-catheter, single-use FDA UDI
Device Name: Intermediate Catheter FDA UDI
Model / Reference: INC-11814-153 FDA UDI
Description: Intermediate Catheter FDA UDI

Identifiers

Catalog Number: INC-11814-153 FDA UDI
Primary DI / UDI-DI: 07613327519372 FDA UDI
510(k) Number: K190338 FDA UDI
K202752 FDA UDI
FDA Product Code: NRY FDA UDI
QJP FDA UDI
GMDN Term: Vascular guide-catheter, single-use 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

FDA UDI

Contains Latex

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

FDA UDI

Dimensions & Sizes

Size: Lumen/Inner Diameter — 0.046 Inch FDA UDI
Length — 153.0 Centimeter FDA UDI

Category: Vascular guide-catheter, single-use Thrombectomy suction catheter

Axs Vecta 46 by Stryker Corp. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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Also classified as Thrombectomy suction catheter.

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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 a44a96aa-dfd6-4018-a4fe-8039ca2d8edf 38 fields · synced May 30, 2026