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Multi-Dop X digital

FDA UDIEUDAMED

Class II (US FDA UDI)

Ref 7882Model Multi-Dop X digital with CO2 measuring module

by Compumedics Germany GmbH

Identity

Trade Name
Multi-Dop X digital with CO2 measuring module EUDAMED
Multi-Dop X digital FDA UDI
Generic Name
Noninvasive vascular ultrasound system, line-powered FDA UDI
Device Name
Ultrasound Doppler Device with CO2 measuring module FDA UDI
Model / Reference
Multi-Dop X digital with CO2 measuring module EUDAMED
7882 EUDAMED
MDX R12 CO2 FDA UDI
Description
Ultrasound Doppler Device with CO2 measuring module FDA UDI

Identifiers

Catalog Number
7882 FDA UDI
Primary DI / UDI-DI
04260493310031 EUDAMEDFDA UDI
Basic UDI-DI
B-04260493310031 EUDAMED
510(k) Number
K051085 FDA UDI
FDA Product Code
IYN FDA UDI
ITX FDA UDI
EMDN Code
Z12040111 BLOOD FLOW METERS EUDAMED
GMDN Term
Noninvasive vascular ultrasound system, line-powered FDA UDI

Classification

Device Class
Class IIa EUDAMED
Class II FDA UDI
Regulation Number
892.1550 FDA UDI
892.1570 FDA UDI
Market of Registration
Germany EUDAMED
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

EUDAMEDFDA UDI

Single Use

No

FDA UDI

Implantable

No

EUDAMEDFDA UDI

Reusable

No

EUDAMED

Contains Latex

No

EUDAMEDFDA UDI

Reprocessed

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

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

Yes

FDA UDI

Category: Invasive vascular ultrasound systemNoninvasive vascular ultrasound system, line-powered

Multi-Dop X digital by Compumedics Germany GmbH — Class II — MDD, FDA UDI — listed in FDA GUDID, EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Noninvasive vascular ultrasound system, line-powered.

Cleared under the same submission

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Unknown

MDD

United States Pending data

FDA UDI

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Manufacturer

Sources (2)

  • FDA UDI 26525e98-3712-4986-91d9-68505fe314ed 36 fields · synced Jul 27, 2026
  • EUDAMED 2ed9e26d-c504-4651-bc2d-405623bc8fc8 61 fields · synced Jul 27, 2026