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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 posts — 6 UDI-DI variants, MDR (SANADEN SRLS)

MD Atlas
SANADEN SRLS

Data from EUDAMED, last updated May 30, 2026

Endodontic posts

80517066306R

6 UDI-DI variants

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

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Manufacturer: SANADEN SRLS

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Device characteristics

Implantable

Identity & classification

Basic UDI-DI: 80517066306R
Device name: Endodontic posts
Device model: Fiberglass Endodontic Post
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: May 13, 2026

Manufacturer & authorised representative

Manufacturer

Name: SANADEN SRLS
SRN: IT-MF-000035916
Country: Italy
Email: info@sanaden.com

Variants by status

UDI-DI variants

6 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01KBMT6EFXVK9SE0DC4GZCNNEB

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

10-2Wa08051706630352
20-2Wh08051706630468
14-2Wa08051706630376
12-2Wa08051706630369
08-2Wa08051706630345
40-2Wh08051706630475