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Dvm 4500

FDA UDI

Class II (US FDA UDI)

by Koven Technology, Inc.

Identity

Trade Name
DVM 4500 FDA UDI
Generic Name
Invasive vascular ultrasound system FDA UDI
Device Name
Doppler blood flowmeter. FDA UDI
Model / Reference
DVM 4500 FDA UDI
Description
Doppler blood flowmeter. FDA UDI

Identifiers

Catalog Number
DVM 4500 FDA UDI
Primary DI / UDI-DI
00894912002180 FDA UDI
510(k) Number
K892707 FDA UDI
FDA Product Code
DPW FDA UDI
GMDN Term
Invasive vascular ultrasound system 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

No

FDA UDI

Single Use

No

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

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI
MRI Safety
MR Unsafe FDA UDI

Category: Invasive vascular ultrasound system

Dvm 4500 by Koven Technology, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Invasive vascular ultrasound system.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Koven Technology, Inc.

Sources (1)

  • FDA UDI 12c2cc7f-4060-481f-b09a-9285986dcb5d 36 fields · synced Jun 9, 2026