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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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Faja abdominal / Abdominal binder — 3 UDI-DI variants, MDR

MD Atlas
C.V. MEDICA, SL

Data from EUDAMED, last updated May 31, 2026

Faja abdominal / Abdominal binder

8427835TF011XG

3 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: 8427835TF011XG
Device name: —
Device model: Faja abdominal / Abdominal binder
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

3 UDI-DI variants

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Applied filters

basicUdiUlid01KRXHJ1DT5AQ96PBCES73Q0HV

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

Abdominal binder large08427835102310
Abdominal binder medium08427835102297
Abdominal binder Small08427835102303