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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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HEPTA — 12 UDI-DI variants, MDR (LID - SOTRAMET)

MD Atlas
LID - SOTRAMET

Data from EUDAMED, last updated May 19, 2026

HEPTA

376036183HEPTAB4

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: LID - SOTRAMET

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 376036183HEPTAB4
Device name: HEPTA
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Jan 22, 2024

Manufacturer & authorised representative

Manufacturer

Name: LID - SOTRAMET
SRN: FR-MF-000014659
Country: France
Email: direction@lid-lamps.com
Phone: + 33 4 42928976

Variants by status

UDI-DI variants

12 UDI-DI variants

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Applied filters

basicUdiUlid01HMRAY9M902B7D2A9391238V6

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

HEPTA03760361831237
HEPTA03760361831190
HEPTA03760361831213
HEPTA03760361831244
HEPTA03760361831169
HEPTA03760361831183
HEPTA03760361831145
HEPTA03760361831138
HEPTA03760361831206
HEPTA03760361831220
HEPTA03760361831152
HEPTA03760361831176