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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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Microprint — 1 UDI-DI variant, MDD (PRO DATA S.r.l.)

MD Atlas
PRO DATA S.r.l.

Data from EUDAMED, last updated May 30, 2026

Microprint

B-08054110360013

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: PRO DATA S.r.l.

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Device characteristics

Measuring function

Legacy certificates

Certificate number: HD 60151130
Type: refdata.legacy.mdd-certificate-type.ii-excluding-4
Notified body: TUV Rheinland Italia SRL (1936)
Validity: May 26, 2024

Identity & classification

Basic UDI-DI: B-08054110360013
Device name: Microprint
Device model: 2.0.XX
Issuing agency: EUDAMED
Legislation: MDD [Directive 93/42/EEC on medical devices]
Risk class: Class IIa
Special device type: refdata.special-mdd-device-type.software
Version date: May 28, 2026

Manufacturer & authorised representative

Manufacturer

Name: PRO DATA S.r.l.
SRN: IT-MF-000029316
Country: Italy
Email: info@prodatasrl.eu

Variants by status

UDI-DI variants

1 UDI-DI variant

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Export results

Applied filters

basicUdiUlid01KSQMKKGGT4SP6AP05NBWRRWW

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

01.2008054110360013