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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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iCONNECT System Cable — 5 UDI-DI variants, MDR (OSYPKA GmbH)

MD Atlas
OSYPKA GmbH

Data from EUDAMED, last updated May 31, 2026

iCONNECT System Cable

4044508iConnectSCS

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: OSYPKA GmbH

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 4044508iConnectSCS
Device name: —
Device model: iCONNECT System Cable
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: May 26, 2026

Manufacturer & authorised representative

Manufacturer

Name: OSYPKA GmbH
SRN: DE-MF-000005610
Country: Germany
Email: ra@osypka.de
Phone: +49 7623 7405 0

Variants by status

UDI-DI variants

5 UDI-DI variants

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Applied filters

basicUdiUlid01KSHZFZKEA3KQ1V6TR0RKPAAK

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

iCONNECT - AMPERE04044508137048
iCONNECT - HAT50004044508137062
iCONNECT - MAESTRO04044508136980
iCONNECT - SMARTABLATE04044508137000
iCONNECT - STOCKERT04044508137024