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Vitale

FDA UDI

Class II (US FDA UDI)

by QXMedical, LLC

Identity

Trade Name
Vitale FDA UDI
Generic Name
Intravascular occluding balloon catheter, image-guided FDA UDI
Device Name
Occlusion Balloon Catheter, 8F compatible FDA UDI
Model / Reference
VITB08 FDA UDI
Description
Occlusion Balloon Catheter, 8F compatible FDA UDI

Identifiers

Catalog Number
VITB08 FDA UDI
Primary DI / UDI-DI
00853892004119 FDA UDI
FDA Product Code
MJN FDA UDI
GMDN Term
Intravascular occluding balloon catheter, image-guided FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
870.4450 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
Balloon Length — 80 Millimeter FDA UDI
Catheter Length — 90 Centimeter FDA UDI
Crossing Profile — 8 French FDA UDI
Introducer Sheath Compatibility — 8 French FDA UDI

Category: Intravascular occluding balloon catheter, image-guided

Vitale by QXMedical, LLC — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Intravascular occluding balloon catheter, image-guided.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
QXMedical, LLC

Sources (1)

  • FDA UDI ef24f08b-dfa0-4591-993c-dc1886fe861b 36 fields · synced Jun 8, 2026