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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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Dualsan PELOTA cuscinetto contenimento… — 2 UDI-DI variants, MDR

MD Atlas
Dual Sanitaly S.p.A. SB

Data from EUDAMED, last updated May 31, 2026

Dualsan PELOTA cuscinetto contenimento ernia

8054382245N5308TH

2 UDI-DI variants

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

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Manufacturer: Dual Sanitaly S.p.A. SB

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 8054382245N5308TH
Device name: Dualsan PELOTA cuscinetto contenimento ernia
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Apr 30, 2026

Manufacturer & authorised representative

Manufacturer

Name: Dual Sanitaly S.p.A. SB
SRN: IT-MF-000052906
Country: Italy
Email: francescorangoni@dualsanitaly.it

Variants by status

UDI-DI variants

2 UDI-DI variants

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Applied filters

basicUdiUlid01KQFAJDJK9EBW6FHQZ2FA627E

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

5N5308X00AA0108054382241171
5N5308X00AA0208054382242703