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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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Terrypad — 6 UDI-DI variants, MDR (Lomed Nederland)

MD Atlas
Lomed Nederland

Data from EUDAMED, last updated May 30, 2026

Terrypad

8718873DV9990ZT

6 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: 8718873DV9990ZT
Device name: Terrypad
Device model: DV 999
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Jan 8, 2024

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

6 UDI-DI variants

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Applied filters

basicUdiUlid01HKM5KZM0HGTWYCDJZ93CKCZM

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

DV 99908718873037031
DV 9990908718873004606
DV 9991008718873004613
DV 9990608718873004590
DV 9990308718873004538
DV 9990508718873004583