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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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STROMATOL — 2 UDI-DI variants, IVDR (Mascia Brunelli S.p.A.)

MD Atlas
Mascia Brunelli S.p.A.

Data from EUDAMED, last updated May 31, 2026

STROMATOL

803373798STROMATOL00032PY

2 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: Mascia Brunelli S.p.A.

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Device characteristics

ReagentProfessional testing

Identity & classification

Basic UDI-DI: 803373798STROMATOL00032PY
Device name: —
Device model: STROMATOL
Issuing agency: GS1
Legislation: IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]
Risk class: IVDR Class A
Version date: Mar 11, 2026

Manufacturer & authorised representative

Manufacturer

Name: Mascia Brunelli S.p.A.
SRN: IT-MF-000009572
Country: Italy
Email: mktg@masciabrunelli.it
Phone: +39 02.252091

Variants by status

UDI-DI variants

2 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01KKE3NV3QG8BB11XT1AVTYV20

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

321200108033737981177
321200S08033737981184