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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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Eagle II — 5 UDI-DI variants, MDR (Vital Pro Kft.)

MD Atlas
Vital Pro Kft.

Data from EUDAMED, last updated May 24, 2026

Eagle II

59991300REF700120VN

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: Vital Pro Kft.

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 59991300REF700120VN
Device name: Eagle II
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Nov 14, 2024

Manufacturer & authorised representative

Manufacturer

Name: Vital Pro Kft.
SRN: HU-MF-000028773
Country: Hungary
Email: vitalprohungary@gmail.com

Variants by status

UDI-DI variants

5 UDI-DI variants

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Applied filters

basicUdiUlid01JCN2R592ZXD86Z8C98WW3N80

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

70012405999130000002
70012605999130000026
70012705999130000033
70012805999130000040
70012505999130000019