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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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HYBRIDknife® flex — 3 UDI-DI variants, MDR (Erbe Elektromedizin GmbH)

MD Atlas
Erbe Elektromedizin GmbH

Data from EUDAMED, last updated May 23, 2026

HYBRIDknife® flex

4050147HYBRIDknifeflex-GS

3 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: Erbe Elektromedizin GmbH

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Device characteristics

Active device

Identity & classification

Basic UDI-DI: 4050147HYBRIDknifeflex-GS
Device name: HYBRIDknife® flex
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIb
Version date: May 13, 2026

Manufacturer & authorised representative

Manufacturer

Name: Erbe Elektromedizin GmbH
SRN: DE-MF-000005498
Country: Germany
Email: Ralf.Mack@erbe-med.com
Phone: 004916093969516

Variants by status

UDI-DI variants

3 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01KRGFD0HJG2VR4T6SEE2VG5CN

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

HYBRIDknife® flex I-Type04050147022973
HYBRIDknife® flex T-Type04050147022942
HYBRIDknife® flex T-Type04050147022959