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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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Instrument — 5 UDI-DI variants, MDR (aap Implantate AG)

MD Atlas
aap Implantate AG

Data from EUDAMED, last updated May 31, 2026

Instrument

40424090085HF

5 UDI-DI variants

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

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Manufacturer: aap Implantate AG

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Device characteristics

Reusable

Identity & classification

Basic UDI-DI: 40424090085HF
Device name: —
Device model: Instrument
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: May 29, 2026

Manufacturer & authorised representative

Manufacturer

Name: aap Implantate AG
SRN: DE-MF-000005994
Country: Germany
Email: info@aap.de
Phone: +4930750190

Variants by status

UDI-DI variants

5 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01KST0ZVEB875Y9ANFKK9DWX11

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

IU 7706-5004042409403606
IU 7710-0004042409227417
IU 7705-0004042409207068
IU 7709-0004042409232152
IU 7706-0004042409210365