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VTI 8 MHZ Disposable Doppler Probe, Straight, Box

FDA UDI

Class II (US FDA UDI)

by Vascular Technology Incorporated

Identity

Trade Name
VTI 8 MHZ Disposable Doppler Probe, Straight, Box FDA UDI
Generic Name
Invasive/noninvasive vascular ultrasound probe FDA UDI
Device Name
Part Number 108260, VTI 8 MHZ Disposable Doppler Probe, Straight, Box FDA UDI
Model / Reference
108260 FDA UDI
Description
Part Number 108260, VTI 8 MHZ Disposable Doppler Probe, Straight, Box FDA UDI

Identifiers

Catalog Number
108260 FDA UDI
Primary DI / UDI-DI
10817122020161 FDA UDI
510(k) Number
K082870 FDA UDI
FDA Product Code
DPW FDA UDI
GMDN Term
Invasive/noninvasive vascular ultrasound probe FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
870.2100 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

Yes

FDA UDI

Category: Invasive/noninvasive vascular ultrasound probe

VTI 8 MHZ Disposable Doppler Probe, Straight, Box by Vascular Technology Incorporated — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Invasive/noninvasive vascular ultrasound probe.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 843d59d3-fe0e-4b2f-83a9-d7c3625cb97a 37 fields · synced May 30, 2026