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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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Soporte moldeable / Flexible support — 4 UDI-DI variants, MDR

MD Atlas
C.V. MEDICA, SL

Data from EUDAMED, last updated May 31, 2026

Soporte moldeable / Flexible support

8427835TF008XT

4 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: C.V. MEDICA, SL

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 8427835TF008XT
Device name: —
Device model: Soporte moldeable / Flexible support
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: May 18, 2026

Manufacturer & authorised representative

Manufacturer

Name: C.V. MEDICA, SL
SRN: ES-MF-000004805
Country: Spain
Email: info@cvmedica.com
Phone: +34 977 89 05 98

Variants by status

UDI-DI variants

4 UDI-DI variants

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Applied filters

basicUdiUlid01KRX61N61WWN03DXGZ97PX46E

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

Flexible support - Large18427835102201
Flexible support – Medium18427835102195
Flexible support neonatal – extra small18427835102171
Flexible support paediatric – small18427835102188