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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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Pall Supor AEF Filter — 6 UDI-DI variants, MDR

MD Atlas
Pall International SARL

Data from EUDAMED, last updated May 23, 2026

Pall Supor AEF Filter

5034480IVFC05NINVE8

6 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: Pall International SARL

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 5034480IVFC05NINVE8
Device name: Pall Supor AEF Filter
Device model: AEF1E
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: May 21, 2025

Manufacturer & authorised representative

Manufacturer

Name: Pall International SARL
SRN: CH-MF-000023177
Country: Switzerland
Email: EURegulatory@cytiva.com

Authorised representative

Name: QbD RepS BV
SRN: BE-AR-000000040
Country: Belgium
Phone: +32 3 844 45 01

Variants by status

UDI-DI variants

6 UDI-DI variants

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Applied filters

basicUdiUlid01JVS5M4NJV4GSZ2K53CF8NJMD

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

PALL Nanodyne ELD filter05034480001306
PALL Nanodyne ELD filter05034480001313
PALL Nanodyne NEO FILTER15034480300949
PALL Nanodyne NEO FILTER15034480001419
PALL Supor AEF Filter05034480308825
Pall Supor™ AEF Filter05034480104373