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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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Qubic Stim — 2 UDI-DI variants, MDR (BIOTRONIK SE & Co. KG)

MD Atlas
BIOTRONIK SE & Co. KG

Data from EUDAMED, last updated May 31, 2026

Qubic Stim

4035479BUDI00056QD

2 UDI-DI variants

MDR [Regulation (EU) 2017/745 on medical devices]Class IIb

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIb
Manufacturer: BIOTRONIK SE & Co. KG

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Device characteristics

Active device

Identity & classification

Basic UDI-DI: 4035479BUDI00056QD
Device name: —
Device model: Qubic Stim
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIb
Version date: May 22, 2026

Manufacturer & authorised representative

Manufacturer

Name: BIOTRONIK SE & Co. KG
SRN: DE-MF-000005049
Country: Germany
Email: info@biotronik.com
Phone: +49 30 68905 0

Variants by status

UDI-DI variants

2 UDI-DI variants

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Applied filters

basicUdiUlid01KS7HF7ZNXHXN1SX78CV6BHYM

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

Qubic Stim - Control unit04035479134778
Qubic Stim - EP Heart Stimulator04035479133429