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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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AGE Reader mu — 1 UDI-DI variant, MDD (DiagnOptics Technologies B.V.)

MD Atlas
DiagnOptics Technologies B.V.

Data from EUDAMED, last updated May 30, 2026

AGE Reader mu

B-08720299268111

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: DiagnOptics Technologies B.V.

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Device characteristics

Active deviceMeasuring function

Legacy certificates

Certificate number: 2085393CE01
Type: refdata.legacy.mdd-certificate-type.v
Notified body: DEKRA Certification B.V. (0344)
Validity: May 1, 2023

Identity & classification

Basic UDI-DI: B-08720299268111
Device name: AGE Reader mu
Device model: AGE Reader mu
Issuing agency: EUDAMED
Legislation: MDD [Directive 93/42/EEC on medical devices]
Risk class: Class IIa
Version date: Oct 1, 2024

Manufacturer & authorised representative

Manufacturer

Name: DiagnOptics Technologies B.V.
SRN: NL-MF-000000431
Country: Netherlands
Email: info@diagnoptics.com
Phone: +31 (0)50 598 0612

Variants by status

UDI-DI variants

1 UDI-DI variant

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Applied filters

basicUdiUlid01J93JAECV33Q55Q379REAJ45E

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

AGE Reader mu08720299268111