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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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Enbio S — 15 UDI-DI variants, MDR (Enbio Technology Sp. z o. o.)

MD Atlas
Enbio Technology Sp. z o. o.

Data from EUDAMED, last updated May 30, 2026

Enbio S

5904165sterylizatoryE2

15 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: Enbio Technology Sp. z o. o.

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Device characteristics

Active device

Identity & classification

Basic UDI-DI: 5904165sterylizatoryE2
Device name: Enbio S
Device model: Enbio S
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Special device type: refdata.special-mdr-device-type.software
Version date: Jul 24, 2023

Manufacturer & authorised representative

Manufacturer

Name: Enbio Technology Sp. z o. o.
SRN: PL-MF-000024063
Country: Poland
Email: lukasz.rogowski@enbio.com

Variants by status

UDI-DI variants

15 UDI-DI variants

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Applied filters

basicUdiUlid01H63RPTQAZDJ4S5A1R20RJWPC

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

Enbio S59041656640512
Enbio S59041656640376
Enbio S (P-EU)59041656640208
Enbio S59041656640130
Enbio S59041656642356
Enbio PRO59041656642592
Enbio S59041656641984
Enbio PRO59041656642424
Enbio S59041656642738
Enbio S59041656640444
Enbio PRO59041656640680
Enbio S59041656642042
Enbio S59041656642288
Enbio S59041656642110
Enbio S59041656640062