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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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Lame Hopper — 12 UDI-DI variants, MDR (Hopper)

MD Atlas
Hopper

Data from EUDAMED, last updated May 19, 2026

Lame Hopper

3770027689HL0127

12 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: Hopper

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 3770027689HL0127
Device name: Lame Hopper
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Aug 24, 2022

Manufacturer & authorised representative

Manufacturer

Name: Hopper
SRN: FR-MF-000024280
Country: France
Email: contact@hopper-accessibility.com
Phone: 0781943427

Variants by status

UDI-DI variants

12 UDI-DI variants

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Applied filters

basicUdiUlid01GB89GKQ5E0VJXDDWY0DEW1FS

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

Lame Hopper Gamme L03770027689034
Lame Hopper Gamme M03770027689027
Lame Hopper Gamme PL03770027689096
Lame Hopper Gamme PM03770027689089
Lame Hopper Gamme PS03770027689072
Lame Hopper Gamme PXL03770027689102
Lame Hopper Gamme PXS03770027689065
Lame Hopper Gamme S03770027689010
Lame Hopper Gamme XL03770027689041
Lame Hopper Gamme XS03770027689003
Lame Hopper Gamme XXL03770027689058
Salomon Sole Blue Fire03770027689119