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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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KEAT MEN — 2 UDI-DI variants, MDR (BEACMED S.R.L.)

MD Atlas
BEACMED S.R.L.

Data from EUDAMED, last updated May 31, 2026

KEAT MEN

805901671KEATMENL6

2 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: BEACMED S.R.L.

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Device characteristics

Active device

Identity & classification

Basic UDI-DI: 805901671KEATMENL6
Device name: KEAT MEN
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: May 2, 2025

Manufacturer & authorised representative

Manufacturer

Name: BEACMED S.R.L.
SRN: IT-MF-000023616
Country: Italy
Email: info@beacmed.eu
Phone: +39038543378

Variants by status

UDI-DI variants

2 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01JT866GEH288SHK7AF59ZAH40

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

KEAT Men08059016710443
RU/KM-PROBE08059016710580