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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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CU-ME-154-1 — 2 UDI-DI variants, MDR (Cuantum Medical Cosmetics SL)

MD Atlas
Cuantum Medical Cosmetics SL

Data from EUDAMED, last updated May 23, 2026

CU-ME-154-1

84370CUME154ED

2 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: Cuantum Medical Cosmetics SL

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 84370CUME154ED
Device name: CU-ME-154-1
Device model: DERM·X Twist Pen 1.2 ml
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Sep 5, 2025

Manufacturer & authorised representative

Manufacturer

Name: Cuantum Medical Cosmetics SL
SRN: ES-MF-000007272
Country: Spain
Email: info@cuantum.me
Phone: +34931283560

Variants by status

UDI-DI variants

2 UDI-DI variants

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Applied filters

basicUdiUlid01K4CH1P5RRK1RY96FQ6T9Y5NY

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

DERM·X08437016047170
DERM·X08437016047194