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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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Ferno SNOGG — 4 UDI-DI variants, MDR (Ferno Slovakia)

MD Atlas
Ferno Slovakia

Data from EUDAMED, last updated May 30, 2026

Ferno SNOGG

8588008129600101SplintsE5

4 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: Ferno Slovakia

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 8588008129600101SplintsE5
Device name: Ferno SNOGG
Device model: Ferno SNOGG
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Apr 6, 2022

Manufacturer & authorised representative

Manufacturer

Name: Ferno Slovakia
SRN: SK-MF-000001474
Country: Slovakia
Email: r.kopacik@ferno.com
Phone: +421 911 652 065

Variants by status

UDI-DI variants

4 UDI-DI variants

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Applied filters

basicUdiUlid01FZZ249DAYWHJ9JY6XQ32S6VH

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

441 TRACTION SPLINT08588008129548
S-2443 TRACTION SPLINT08588008129562
S-2444 TRACTION SPLINT08588008129555
Splint08588008129029