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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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MIR102 — 6 UDI-DI variants, MDR

MD Atlas
MIR - Medical International Research S.p.A.

Data from EUDAMED, last updated May 31, 2026

MIR102

805299032102DF

6 UDI-DI variants

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

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Manufacturer: MIR - Medical International Research S.p.A.

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Device characteristics

Active device

Identity & classification

Basic UDI-DI: 805299032102DF
Device name: —
Device model: MIR102
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: May 22, 2026

Manufacturer & authorised representative

Manufacturer

Name: MIR - Medical International Research S.p.A.
SRN: IT-MF-000014026
Country: Italy
Email: mir@spirometry.com
Phone: +39 06 22754777

Variants by status

UDI-DI variants

6 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01KS819QYY05ZTCSGD3RDH9XZT

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

91402208052990320455
914022T08052990320462
90402208052990322176
91402008052990320509
914020T08052990320516
90402008052990322169