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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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NEOPUMP — 57 UDI-DI variants, MDR (Adria Med S.r.l.)

MD Atlas
Adria Med S.r.l.

Data from EUDAMED, last updated May 31, 2026

NEOPUMP

80522047103EASYNMX

57 UDI-DI variants

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

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIb
Manufacturer: Adria Med S.r.l.

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Device characteristics

Active deviceAdministers medicine

Identity & classification

Basic UDI-DI: 80522047103EASYNMX
Device name: NEOPUMP
Device model: NST
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIb
Version date: Jan 12, 2026

Manufacturer & authorised representative

Manufacturer

Name: Adria Med S.r.l.
SRN: IT-MF-000020866
Country: Italy
Email: nico.diflorio@adriamed.com
Phone: +390858886011

Variants by status

UDI-DI variants

57 UDI-DI variants

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Applied filters

basicUdiUlid01KES8CWZS4ZTMK537Z5C354HF

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

NEOPUMP08052204713264
NEOPUMP08052204712588
NEOPUMP08052204712687
NEOPUMP08052204712717
NEOPUMP08052204714025
NEOPUMP08052204713240
NEOPUMP08052204713127

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