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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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ESTREMITÀ PER ANELLI DI FISSAGGIO PER… — 3 UDI-DI variants, MDR

MD Atlas
PERIDENT DENTAL PRODUCTS s.r.l.

Data from EUDAMED, last updated May 30, 2026

ESTREMITÀ PER ANELLI DI FISSAGGIO PER MATRICI

805697705048481R02YU

3 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: PERIDENT DENTAL PRODUCTS s.r.l.

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 805697705048481R02YU
Device name: ESTREMITÀ PER ANELLI DI FISSAGGIO PER MATRICI
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: PERIDENT DENTAL PRODUCTS s.r.l.
SRN: IT-MF-000044166
Country: Italy
Email: quality@perident.it
Phone: +39 055 696540

Variants by status

UDI-DI variants

3 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01KPQHWC3A34YB5DQCZZEB0PK3

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

355008056977050205
355208056977050229
355108056977050212