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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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1117 — 1 UDI-DI variant, MDD

MD Atlas
Przedsiębiorstwo Handlowo-Usługowe "Technomex" Sp. z o.o.

Data from EUDAMED, last updated May 30, 2026

1117

B-05904507654061

1 UDI-DI variant

MDD [Directive 93/42/EEC on medical devices]Class IIa

Legislation: MDD [Directive 93/42/EEC on medical devices]
Risk class: Class IIa
Manufacturer: Przedsiębiorstwo Handlowo-Usługowe "Technomex" Sp. z o.o.

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Device characteristics

Active device

Legacy certificates

Certificate number: 84952734-30
Type: refdata.legacy.mdd-certificate-type.v
Notified body: TÜV Rheinland LGA Products GmbH (0197)
Validity: May 26, 2024

Identity & classification

Basic UDI-DI: B-05904507654061
Device name: —
Device model: 1117
Issuing agency: EUDAMED
Legislation: MDD [Directive 93/42/EEC on medical devices]
Risk class: Class IIa
Version date: Aug 12, 2024

Manufacturer & authorised representative

Manufacturer

Name: Przedsiębiorstwo Handlowo-Usługowe "Technomex" Sp. z o.o.
SRN: PL-MF-000038261
Country: Poland
Email: biuro@technomex.pl
Phone: +48324010350

Variants by status

UDI-DI variants

1 UDI-DI variant

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Applied filters

basicUdiUlid01J52WCHEHG9S0T9ZA81QRRXXX

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

0150140905904507654061