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Our data is continuously updated and sourced from EUDAMED, the European database for medical devices and in vitro diagnostics.

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Medistim Doppler Probe — 1 UDI-DI variant, MDD (Medistim ASA)

MD Atlas
Medistim ASA

Data from EUDAMED, last updated May 30, 2026

Medistim Doppler Probe

B-07070554100740

1 UDI-DI variant

MDD [Directive 93/42/EEC on medical devices]Class III

Legislation: MDD [Directive 93/42/EEC on medical devices]
Risk class: Class III
Manufacturer: Medistim ASA

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Device characteristics

Active device

Legacy certificates

Certificate number: 242113-2017-CE-NOR-NA-PS
Type: refdata.legacy.mdd-certificate-type.ii-4
Notified body: DNV Product Assurance AS (2460)
Validity: May 27, 2024

Identity & classification

Basic UDI-DI: B-07070554100740
Device name: Medistim Doppler Probe
Device model: PD110752
Issuing agency: EUDAMED
Legislation: MDD [Directive 93/42/EEC on medical devices]
Risk class: Class III
Version date: Nov 7, 2023

Manufacturer & authorised representative

Manufacturer

Name: Medistim ASA
SRN: NO-MF-000002741
Country: Norway
Email: medistim@medistim.com
Phone: +47 23 05 96 60

Variants by status

UDI-DI variants

1 UDI-DI variant

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Applied filters

basicUdiUlid01HEMMAB171FAJ8PQ34TWZ072T

Format

Summary

29 columns included

Trade name
Basic UDI-DI
UDI-DI code
Risk category
Applicable legislation
Status
Organization name
SRN
Reference / catalog number
Additional product description
Intended medical purpose
Placed on the market (country)
Market info update date
Sterile
Single use
Contains latex
Reprocessed single-use
Direct marking
CMR substance
Endocrine disruptor
Annex XVI applicable
Sterilization
OEM applicable
EMDN codes
Last updated
Basic UDI-DI device name
Basic UDI-DI device model
Basic UDI-DI implantable
Basic UDI-DI reagent

Medistim Doppler Probe07070554100740