← Back to catalogue

Tubing Kit - Stroke

FDA UDI

Class II (US FDA UDI)

by Microvention Inc.

Identity

Trade Name
Tubing Kit - Stroke FDA UDI
Generic Name
Surgical irrigation/aspiration tubing set FDA UDI
Device Name
Tubing Kit - Stroke FDA UDI
Model / Reference
MVTK110 FDA UDI
Description
Tubing Kit - Stroke FDA UDI

Identifiers

Catalog Number
MVTK110 FDA UDI
Primary DI / UDI-DI
00816777026705 FDA UDI
FDA Product Code
BYY FDA UDI
GMDN Term
Surgical irrigation/aspiration tubing set FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
880.6740 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

Yes

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

Category: Surgical irrigation/aspiration tubing set

Tubing Kit - Stroke by Microvention Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Surgical irrigation/aspiration tubing set.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Microvention Inc.

Sources (1)

  • FDA UDI 4008b1fa-57b5-4c09-80bb-a846068f090b 36 fields · synced May 31, 2026