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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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TESTRAPIDQY — 10 UDI-DI variants, IVDR (Microbiol S.r.l.)

MD Atlas
Microbiol S.r.l.

Data from EUDAMED, last updated May 30, 2026

TESTRAPIDQY

8057920RAPIDTESTQY

10 UDI-DI variants

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

Legislation: IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]
Risk class: IVDR Class A
Manufacturer: Microbiol S.r.l.

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Device characteristics

ReagentProfessional testing

Identity & classification

Basic UDI-DI: 8057920RAPIDTESTQY
Device name: TESTRAPIDQY
Issuing agency: GS1
Legislation: IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]
Risk class: IVDR Class A
Version date: Apr 13, 2026

Manufacturer & authorised representative

Manufacturer

Name: Microbiol S.r.l.
SRN: IT-MF-000052547
Country: Italy
Email: andrea.murgia@microbiol.it
Phone: +39 070 247162

Variants by status

UDI-DI variants

10 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01KP3JFK25Z5BT1F4D2X3GZTRR

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

M.10.5108057920720985
M.10.3308057920720961
M.10.3208057920720954
M.10.3908057920720978
O.10.6508057920721036
O.10.6008057920721043
O.10.7008057920721050
O.10.7108057920721067
K.301-12008057920720824
K.30108057920720817