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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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FLUFSAN ACTIVE PANTS — 5 UDI-DI variants, MDR (EUROPROSAN S.P.A.)

MD Atlas
EUROPROSAN S.P.A.

Data from EUDAMED, last updated May 30, 2026

FLUFSAN ACTIVE PANTS

8015013FLPOAC50N8

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: EUROPROSAN S.P.A.

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 8015013FLPOAC50N8
Device name: FLUFSAN ACTIVE PANTS
Device model: Adult Incontinence pants, single use
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Feb 13, 2025

Manufacturer & authorised representative

Manufacturer

Name: EUROPROSAN S.P.A.
SRN: IT-MF-000009972
Country: Italy
Email: info@europrosan.com
Phone: +390331367111

Variants by status

UDI-DI variants

5 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01JKZV36Z2689JAPGZ7TD67KTY

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

50141508015013501415
50146008015013501460
50246708015013502467
50101908015013501019
50142208015013501422