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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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TRUE FLOW RDB — 1 UDI-DI variant, MDD

MD Atlas
MED EUROPE EUROPEAN MEDICAL SUPPLIES SRL

Data from EUDAMED, last updated May 31, 2026

TRUE FLOW RDB

B-08033609527175

1 UDI-DI variant

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

Legislation: MDD [Directive 93/42/EEC on medical devices]
Risk class: Class IIa
Manufacturer: MED EUROPE EUROPEAN MEDICAL SUPPLIES SRL

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Device characteristics

No device characteristics flagged

Legacy certificates

Certificate number: MED 9827-A
Type: refdata.legacy.mdd-certificate-type.ii-excluding-4
Notified body: KIWA CERMET ITALIA S.P.A. (0476)
Validity: Mar 24, 2023

Identity & classification

Basic UDI-DI: B-08033609527175
Device name: TRUE FLOW RDB
Issuing agency: EUDAMED
Legislation: MDD [Directive 93/42/EEC on medical devices]
Risk class: Class IIa
Version date: Jan 8, 2026

Manufacturer & authorised representative

Manufacturer

Name: MED EUROPE EUROPEAN MEDICAL SUPPLIES SRL
SRN: IT-MF-000026962
Country: Italy
Email: info@medeurope.eu
Phone: +39 051810572

Variants by status

UDI-DI variants

1 UDI-DI variant

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Applied filters

basicUdiUlid01KEEDXJXD5HNNB2X3XV163G3F

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

RDB-0AM08033609527175