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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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Pure Gel Ring — 3 UDI-DI variants, MDR

MD Atlas
Fresco International 2005, S.A.

Data from EUDAMED, last updated May 23, 2026

Pure Gel Ring

84350579F000412C

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: Fresco International 2005, S.A.

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 84350579F000412C
Device name: Pure Gel Ring
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: May 7, 2026

Manufacturer & authorised representative

Manufacturer

Name: Fresco International 2005, S.A.
SRN: ES-MF-000010728
Country: Spain
Email: calidad2@fresco.es

Variants by status

UDI-DI variants

3 UDI-DI variants

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Applied filters

basicUdiUlid01KR1R58SH1Y5YGDXMZ4CRMNWT

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

Cone for 5th toe05206680001213
Pure Gel Ring, Large05206680001206
Pure Gel Ring, Small05206680001190