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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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iMED Tooth Protector — 4 UDI-DI variants, MDR (iMED ApS)

MD Atlas
iMED ApS

Data from EUDAMED, last updated May 31, 2026

iMED Tooth Protector

5745000816TPTPE7N

4 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: iMED ApS

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 5745000816TPTPE7N
Device name: iMED Tooth Protector
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Mar 28, 2025

Manufacturer & authorised representative

Manufacturer

Name: iMED ApS
SRN: DK-MF-000032070
Country: Denmark
Email: mail@i-MED.dk
Phone: +45 2 999 82 22

Variants by status

UDI-DI variants

4 UDI-DI variants

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Applied filters

basicUdiUlid01JQDTV7D71CXHYPC4FZP1CPB8

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

19-100005745000816019
iMED Tooth Protector, double05745000816026
64001205745000816002
ME12660705745000816033