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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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Pro Orthic Footrise — 5 UDI-DI variants, MDR (Lomed Nederland)

MD Atlas
Lomed Nederland

Data from EUDAMED, last updated May 30, 2026

Pro Orthic Footrise

871887300573LC

5 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: Lomed Nederland

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 871887300573LC
Device name: Pro Orthic Footrise
Device model: PO 31802
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Jan 20, 2025

Manufacturer & authorised representative

Manufacturer

Name: Lomed Nederland
SRN: NL-MF-000032807
Country: Netherlands
Email: marketing@lomed.com
Phone: 0880900300

Variants by status

UDI-DI variants

5 UDI-DI variants

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Applied filters

basicUdiUlid01JJ1JR4V1W9A9RD7TCVCYN84J

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

PO 3180208718873005733
PO 31802 L08718873005726
PO 31802 M08718873005719
PO 31802 S08718873005702
PO 31802 XS08718873005696