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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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Pixie Skin Tag — 3 UDI-DI variants, MDR (Oystershell NV)

MD Atlas
Oystershell NV

Data from EUDAMED, last updated May 23, 2026

Pixie Skin Tag

5410765PixieSkinTagSM

3 UDI-DI variants

MDR [Regulation (EU) 2017/745 on medical devices]Class IIa

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Manufacturer: Oystershell NV

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 5410765PixieSkinTagSM
Device name: Pixie Skin Tag
Device model: X92001673
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: Nov 21, 2025

Manufacturer & authorised representative

Manufacturer

Name: Oystershell NV
SRN: BE-MF-000011797
Country: Belgium
Email: regulatory@oystershell.be
Phone: 0032.09.377.24.85

Variants by status

UDI-DI variants

3 UDI-DI variants

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Applied filters

basicUdiUlid01KAKMHGXFBVJAF6X29VQ4FH4C

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

0701168705410765008510
0701168405410765008480
0701168505410765008497