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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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PD DETECT — 4 UDI-DI variants, IVDR (AIDA GmbH)

MD Atlas
AIDA GmbH

Data from EUDAMED, last updated May 23, 2026

PD DETECT

42601586PDDETECTSE

4 UDI-DI variants

IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]IVDR Class B

Legislation: IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]
Risk class: IVDR Class B
Manufacturer: AIDA GmbH

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Device characteristics

Professional testingHuman tissues / cells

Identity & classification

Basic UDI-DI: 42601586PDDETECTSE
Device name: PD DETECT
Issuing agency: GS1
Legislation: IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]
Risk class: IVDR Class B
Version date: Apr 9, 2026

Manufacturer & authorised representative

Manufacturer

Name: AIDA GmbH
SRN: DE-MF-000040784
Country: Germany
Email: registrations@aida-diagnostics.com

Variants by status

UDI-DI variants

4 UDI-DI variants

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Applied filters

basicUdiUlid01KN6G31BYJAZ2HMMXYS2X0V6N

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

SAA-001_0204260158683531
SAA-001_2004260158683500
SAA-002_0204260158683548
SAA-002_2004260158683524