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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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Endodontic sponges — 55 UDI-DI variants, MDR (Larident SRL)

MD Atlas
Larident SRL

Data from EUDAMED, last updated May 30, 2026

Endodontic sponges

80530498ESB2

55 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: Larident SRL

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 80530498ESB2
Device name: Endodontic sponges
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Apr 21, 2026

Manufacturer & authorised representative

Manufacturer

Name: Larident SRL
SRN: IT-MF-000007807
Country: Italy
Email: rolleri@larident.it

Variants by status

UDI-DI variants

55 UDI-DI variants

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Applied filters

basicUdiUlid01KPQAN6P5372ZAP1FKHNFNCMC

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

C90-WIEDER (916243)08050503880168
C92-G.LINE08050503881523
C90-G.LINE08050503880007
C90-UNODENT08050503880137
C92-UNODENT08050503881639

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