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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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Peristomal Paste — 5 UDI-DI variants, MDR (Avery Dennison Medical)

MD Atlas
Avery Dennison Medical

Data from EUDAMED, last updated May 24, 2026

Peristomal Paste

081713801TF014XX

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: Avery Dennison Medical

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 081713801TF014XX
Device name: Peristomal Paste
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: May 30, 2024

Manufacturer & authorised representative

Manufacturer

Name: Avery Dennison Medical
SRN: IE-MF-000001926
Country: Ireland
Email: elaine.minagh@eu.averydennison.com
Phone: +353 43 33 49586

Variants by status

UDI-DI variants

5 UDI-DI variants

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Applied filters

basicUdiUlid01HZ587KJ8PY7G83TXTJ7PW7NK

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

Superfiller00817138015482
Superfiller00817138015505
Superfiller00817138015475
Superfiller00817138015499
FM0016000817138012269