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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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MSwab — 4 UDI-DI variants, IVDR (Copan Italia S.P.A.)

MD Atlas
Copan Italia S.P.A.

Data from EUDAMED, last updated May 31, 2026

MSwab

80533260CD0350AM004AE

4 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: Copan Italia S.P.A.

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Device characteristics

Professional testing

Identity & classification

Basic UDI-DI: 80533260CD0350AM004AE
Device name: MSwab
Issuing agency: GS1
Legislation: IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]
Risk class: IVDR Class A
Version date: May 26, 2026

Manufacturer & authorised representative

Manufacturer

Name: Copan Italia S.P.A.
SRN: IT-MF-000022535
Country: Italy
Email: regulatory.affairs@copangroup.com

Variants by status

UDI-DI variants

4 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01KSHZRMTA0HPEEBJX5GR2Q5WD

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

Mswab08053326009938
Mswab08053326007712
MSwab08053326007774
MSwab08053326011092