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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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VENDAS ELÁSTICAS DE CREPÉ — 19 UDI-DI variants, MDR

MD Atlas
Ortopedia y Cirugía, S.L.

Data from EUDAMED, last updated May 23, 2026

VENDAS ELÁSTICAS DE CREPÉ

843508159700F8

19 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: Ortopedia y Cirugía, S.L.

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 843508159700F8
Device name: VENDAS ELÁSTICAS DE CREPÉ
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: Ortopedia y Cirugía, S.L.
SRN: ES-MF-000016977
Country: Spain
Email: lab@laboratoriooc.com
Phone: +34 93 835 81 61

Variants by status

UDI-DI variants

19 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01KRWTN3PQ5P4NZ4JKTXCWWBY9

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

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970508435081597057
310-000508435081500057
310-000408435081500040
310-000308435081500033
310-000208435081500026
310-000108435081500019