Axs Vecta 71

FDA UDI

Class II (US FDA UDI)

by Stryker Corp.

Identity

Trade Name: AXS VECTA 71 FDA UDI
Generic Name: Thrombectomy suction catheter FDA UDI
Device Name: Intermediate Catheter FDA UDI
Model / Reference: INC-11129-115 FDA UDI
Description: Intermediate Catheter FDA UDI

Identifiers

Catalog Number: INC-11129-115 FDA UDI
Primary DI / UDI-DI: 07613327459210 FDA UDI
510(k) Number: K172167 FDA UDI
K190212 FDA UDI
K190833 FDA UDI
K191768 FDA UDI
K200206 FDA UDI
FDA Product Code: DQY FDA UDI
NRY FDA UDI
QJP FDA UDI
DTL FDA UDI
DYB FDA UDI
GMDN Term: Thrombectomy suction catheter FDA UDI

Classification

Device Class: Class II FDA UDI
Regulation Number: 870.1250 FDA UDI
870.4290 FDA UDI
870.1340 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: Length — 115.0 Centimeter FDA UDI
Lumen/Inner Diameter — 0.071 Inch FDA UDI

Category: Thrombectomy suction catheter

Axs Vecta 71 by Stryker Corp. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Thrombectomy suction catheter.

Symphony™ ProHelix™ — IMPERATIVE CARE INC. · Class II
Prodigy™ Catheter — IMPERATIVE CARE INC. · Class II
Symphony™ Advance™ Long Dilator — IMPERATIVE CARE INC. · Class II
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

K172167 also covers:

K190212 also covers:

K190833 also covers:

K191768 also covers:

K200206 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 1c071ad6-0db1-4797-a098-1bc1b9fb73cd 38 fields · synced May 30, 2026