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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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Nitril DAILY S — 4 UDI-DI variants, MDR (Wirfly s.r.l.)

MD Atlas
Wirfly s.r.l.

Data from EUDAMED, last updated May 31, 2026

Nitril DAILY S

805194498000ES

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: Wirfly s.r.l.

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 805194498000ES
Device name: Nitril DAILY S
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Jul 17, 2025

Manufacturer & authorised representative

Manufacturer

Name: Wirfly s.r.l.
SRN: IT-MF-000048497
Country: Italy
Email: info@wirfly.com

Variants by status

UDI-DI variants

4 UDI-DI variants

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Applied filters

basicUdiUlid01K0BYT0Q2DK8S1VSCAR6S18CT

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

MV480-S08051944980042
MV480-M08051944980059
MV480-L08051944980066
MV480-XL08051944980073