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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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ELITE 1600 PLUS — 1 UDI-DI variant, MDR (GRUPPO MAIORFLEX SRLS)

MD Atlas
GRUPPO MAIORFLEX SRLS

Data from EUDAMED, last updated May 30, 2026

ELITE 1600 PLUS

805475268ELITE1600PLUSC4

1 UDI-DI variant

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

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Manufacturer: GRUPPO MAIORFLEX SRLS

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 805475268ELITE1600PLUSC4
Device name: ELITE 1600 PLUS
Device model: ELITE 1600 PLUS
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Jul 5, 2024

Manufacturer & authorised representative

Manufacturer

Name: GRUPPO MAIORFLEX SRLS
SRN: IT-MF-000033863
Country: Italy
Email: info@gruppomaiorflex.it
Phone: +39 0833832129

Variants by status

UDI-DI variants

1 UDI-DI variant

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Applied filters

basicUdiUlid01J21Q6JGRMBAC1ST3K5PEK1B5

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

ELITE 1600 PLUS08054752680036