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Trevo NXT

FDA UDI

Class II (US FDA UDI)

by Stryker Corp.

Identity

Trade Name
Trevo NXT FDA UDI
Generic Name
Thrombectomy suction catheter FDA UDI
Device Name
ProVue Retriever FDA UDI
Model / Reference
90313 FDA UDI
Description
ProVue Retriever FDA UDI

Identifiers

Catalog Number
90313 FDA UDI
Primary DI / UDI-DI
07613327299939 FDA UDI
510(k) Number
K192207 FDA UDI
K200117 FDA UDI
FDA Product Code
NRY FDA UDI
POL FDA UDI
GMDN Term
Thrombectomy suction catheter FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
870.1250 FDA UDI
882.5600 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

Category: Thrombectomy suction catheter

Trevo NXT by Stryker Corp. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Thrombectomy suction catheter.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Stryker Corp.

Sources (1)

  • FDA UDI 38508570-9e33-46f2-8859-f28d6483c16a 38 fields · synced May 30, 2026