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Summit Doppler

FDA UDI

Class II (US FDA UDI)

by CooperSurgical, Inc.

Identity

Trade Name
Summit Doppler FDA UDI
Generic Name
Noninvasive vascular ultrasound system FDA UDI
Device Name
LifeDop 350R Tabletop Doppler with 8.0 MHz Vascular Probe FDA UDI
Model / Reference
L350R-SD8 FDA UDI
Description
LifeDop 350R Tabletop Doppler with 8.0 MHz Vascular Probe FDA UDI

Identifiers

Primary DI / UDI-DI
00888937002423 FDA UDI
510(k) Number
K090499 FDA UDI
FDA Product Code
MAA FDA UDI
GMDN Term
Noninvasive vascular ultrasound system FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
884.2660 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

Category: Noninvasive vascular ultrasound system

Summit Doppler by CooperSurgical, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Noninvasive vascular ultrasound system.

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 41af576d-f9fa-4d9e-ba9f-bbbfdb7cb877 34 fields · synced Jun 9, 2026