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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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LungCT/BoneCT — 2 UDI-DI variants, MDR (GLEAMER)

MD Atlas
GLEAMER

Data from EUDAMED, last updated May 19, 2026

LungCT/BoneCT

37700208390006L2

2 UDI-DI variants

MDR [Regulation (EU) 2017/745 on medical devices]Class IIa

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Manufacturer: GLEAMER

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Device characteristics

Active device

Identity & classification

Basic UDI-DI: 37700208390006L2
Device name: LungCT/BoneCT
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Special device type: refdata.special-mdr-device-type.software
Version date: May 1, 2025

Manufacturer & authorised representative

Manufacturer

Name: GLEAMER
SRN: FR-MF-000011358
Country: France
Email: qara@gleamer.ai

Variants by status

UDI-DI variants

2 UDI-DI variants

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Applied filters

basicUdiUlid01JT5DY908YARKC19N1KAFMRM8

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

BoneCT03770020839139
LungCT03770020839122