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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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EF LINE — 89 UDI-DI variants, MDR (ORTHOPLUS)

MD Atlas
ORTHOPLUS

Data from EUDAMED, last updated May 19, 2026

EF LINE

3665614-EF-LINE-DN

89 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: ORTHOPLUS

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 3665614-EF-LINE-DN
Device name: —
Device model: EF LINE
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Oct 20, 2022

Manufacturer & authorised representative

Manufacturer

Name: ORTHOPLUS
SRN: FR-MF-000007297
Country: France
Email: qualite@orthoplus.fr
Phone: +33 1 69 41 90 28

Variants by status

UDI-DI variants

89 UDI-DI variants

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Applied filters

basicUdiUlid01FKQMD2WP20RC0MQWMAJQH4DE

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

INTERCEPTEUR LABIAL PEDIATRIC WITH STOP PINK03665614595105
INTERCEPTEUR LABIAL PEDIATRIC WITH STOP TRANSLUCENT03665614595099
INTERCEPTEUR LABIAL PINK03665614595051
INTERCEPTEUR LABIAL TRANSLUCENT03665614595013
MYO FLEX03665614599097
MYO TONIC03665614599103
D594 030H03665614594085
D594 03003665614594078
D594 032H03665614594108
D594 03203665614594092
TMO03665614599059
TMO Petit03665614599066
TMO PLUS03665614599073
TMO PLUS Petit03665614599080

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