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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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Codera anatómica — 4 UDI-DI variants, MDR (TEXTIL ELASTICO, S.L.U)

MD Atlas
TEXTIL ELASTICO, S.L.U

Data from EUDAMED, last updated May 23, 2026

Codera anatómica

8425693NC850W3

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: TEXTIL ELASTICO, S.L.U

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 8425693NC850W3
Device name: Codera anatómica
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: May 27, 2025

Manufacturer & authorised representative

Manufacturer

Name: TEXTIL ELASTICO, S.L.U
SRN: ES-MF-000000381
Country: Spain
Email: calidad@textil-elastico.com

Variants by status

UDI-DI variants

4 UDI-DI variants

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Applied filters

basicUdiUlid01JW8P52VT7G6V0J47AS3HB4B8

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

NC850-A-S08425693002001
NC850-A-XL08425693002032
NC850-A-M08425693002018
NC850-A-L08425693002025