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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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GreenDrain — 8 UDI-DI variants, MDR (Green Drain Europe ApS)

MD Atlas
Green Drain Europe ApS

Data from EUDAMED, last updated May 23, 2026

GreenDrain

5745001471GreenDrainMDRJD

8 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: Green Drain Europe ApS

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 5745001471GreenDrainMDRJD
Device name: GreenDrain
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Apr 21, 2026

Manufacturer & authorised representative

Manufacturer

Name: Green Drain Europe ApS
SRN: DK-MF-000052289
Country: Denmark
Email: info@greendrains.eu
Phone: +4553539595

Variants by status

UDI-DI variants

8 UDI-DI variants

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Applied filters

basicUdiUlid01KPRC75W5FXFH8JK04GZJZRV8

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

GD6-M05745001471071
GD4-M05745001471057
GD3-M05745001471033
GD35-M05745001471040
GD5-M05745001471064
GD15-M05745001471019
GD2-M05745001471026
GD125-M 05745001471002