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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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GMOTIO — 8 UDI-DI variants, MDR (PROMOTAL)

MD Atlas
PROMOTAL

Data from EUDAMED, last updated May 19, 2026

GMOTIO

37014094GMOTIOGF

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: PROMOTAL

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Device characteristics

Active device

Identity & classification

Basic UDI-DI: 37014094GMOTIOGF
Device name: —
Device model: GMOTIO
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Sep 17, 2025

Manufacturer & authorised representative

Manufacturer

Name: PROMOTAL
SRN: FR-MF-000001666
Country: France
Email: jllesaint@promotal.com

Variants by status

UDI-DI variants

8 UDI-DI variants

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Applied filters

basicUdiUlid01K5BWZZ09R4RA6RBH0J75WVCB

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

PROMOTAL03701409401227
PROMOTAL03701409401098
PROMOTAL03701409401210
PROMOTAL03701409401234
PROMOTAL03701409400497
PROMOTAL03701409400503
PROMOTAL03701409400480
PROMOTAL03701409401104