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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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Sponges Nonwoven, non-sterile — 5 UDI-DI variants, MDR

MD Atlas
OneMed Group Oy

Data from EUDAMED, last updated May 23, 2026

Sponges Nonwoven, non-sterile

6438129B0012GZ

5 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: OneMed Group Oy

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 6438129B0012GZ
Device name: Sponges Nonwoven, non-sterile
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Jan 4, 2022

Manufacturer & authorised representative

Manufacturer

Name: OneMed Group Oy
SRN: FI-MF-000000642
Country: Finland
Email: eudamed.onemedgroup@onemed.com

Variants by status

UDI-DI variants

5 UDI-DI variants

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Applied filters

basicUdiUlid01FRJN05ZQJZ3TS638TJZ8XQQ1

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

Embra® Optimia Nonwoven round sponges, diam. 30 mm06438129370348
Embra® Optimia Nonwoven round sponges, diam. 40 mm06438129370355
Embra® Optimia Nonwoven round sponges, diam. 50 mm06438129370362
Embra® Optimia Triangular nonwoven sponges, 30x30x30 mm06438129170375
SELEFA Nonwoven round sponges, diam. 70 mm, non-sterile06438129352320