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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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Auditbase — 1 UDI-DI variant, MDR (Auditdata A/S)

MD Atlas
Auditdata A/S

Data from EUDAMED, last updated May 31, 2026

Auditbase

05711781DHF2003-12Z

1 UDI-DI variant

MDR [Regulation (EU) 2017/745 on medical devices]Class IIb

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIb
Manufacturer: Auditdata A/S

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 05711781DHF2003-12Z
Device name: Auditbase
Device model: 2003 Auditbase
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIb
Special device type: refdata.special-mdr-device-type.software
Version date: May 28, 2024

Manufacturer & authorised representative

Manufacturer

Name: Auditdata A/S
SRN: DK-MF-000011415
Country: Denmark
Email: compliance@auditdata.com

Variants by status

UDI-DI variants

1 UDI-DI variant

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Applied filters

basicUdiUlid01HYZDB680EN37038RFQGM4GQH

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

2003 Auditbase05711781002064