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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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Ovelle White Soft Paraffin — 2 UDI-DI variants, MDR (Ovelle Ltd)

MD Atlas
Ovelle Ltd

Data from EUDAMED, last updated May 24, 2026

Ovelle White Soft Paraffin

50989281119UN

2 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: Ovelle Ltd

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 50989281119UN
Device name: Ovelle White Soft Paraffin
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Nov 10, 2025

Manufacturer & authorised representative

Manufacturer

Name: Ovelle Ltd
SRN: IE-MF-000016705
Country: Ireland
Email: info@gardinerfamilyapothecary.com
Phone: +353 (0)42 9332304

Variants by status

UDI-DI variants

2 UDI-DI variants

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Applied filters

basicUdiUlid01K9Q6YAVZJGHKBFH1W08JNY8A

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

Ovelle White Soft Paraffin 100g50989280012192
Ovelle White Soft Paraffin 500g50989280011195