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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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BEK — 3 UDI-DI variants, MDR (Neatech.it)

MD Atlas
Neatech.it

Data from EUDAMED, last updated May 30, 2026

BEK

805538493S205CH

3 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: Neatech.it

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 805538493S205CH
Device name: BEK
Device model: S205
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Jan 18, 2024

Manufacturer & authorised representative

Manufacturer

Name: Neatech.it
SRN: IT-MF-000031601
Country: Italy
Email: info@neatech.it
Phone: +390815551946

Variants by status

UDI-DI variants

3 UDI-DI variants

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Applied filters

basicUdiUlid01HME1T0QE2HD3QQYHAB3NZARH

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

S20508055384930223
S20508055384930209
S20508055384930216