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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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4DFLapTM — 2 UDI-DI variants, MDR (PlantTec Medical GmbH)

MD Atlas
PlantTec Medical GmbH

Data from EUDAMED, last updated May 31, 2026

4DFLapTM

4260419634DFLapZ2

2 UDI-DI variants

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

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Manufacturer: PlantTec Medical GmbH

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 4260419634DFLapZ2
Device name: 4DFLapTM
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: May 28, 2026

Manufacturer & authorised representative

Manufacturer

Name: PlantTec Medical GmbH
SRN: DE-MF-000005921
Country: Germany
Email: info@planttec-medical.de
Phone: +4941313942360

Variants by status

UDI-DI variants

2 UDI-DI variants

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Applied filters

basicUdiUlid01KSPWP6RQZW6RWR99DDG49CZE

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

LA0014-EU04260419631035
LA0038-EU04260419631080