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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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SUPROshoulder Pro — 2 UDI-DI variants, MDR (OPED GmbH)

MD Atlas
OPED GmbH

Data from EUDAMED, last updated May 31, 2026

SUPROshoulder Pro

4046618Y0606SD-PED

2 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: OPED GmbH

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 4046618Y0606SD-PED
Device name: SUPROshoulder Pro
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Apr 9, 2026

Manufacturer & authorised representative

Manufacturer

Name: OPED GmbH
SRN: DE-MF-000008286
Country: Germany
Email: info@oped.de

Variants by status

UDI-DI variants

2 UDI-DI variants

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Applied filters

basicUdiUlid01KNRXPJX8M8E541NHPRY2707S

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

SUSD-06-2-S/M04046618161517
SUSD-06-2-L/XL04046618161463