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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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BANDEJAS — 129 UDI-DI variants, MDR (Ivalmed S.L.)

MD Atlas
Ivalmed S.L.

Data from EUDAMED, last updated May 23, 2026

BANDEJAS

84357608BANDEJASXH

129 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: Ivalmed S.L.

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Device characteristics

Reusable

Identity & classification

Basic UDI-DI: 84357608BANDEJASXH
Device name: BANDEJAS
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Apr 10, 2024

Manufacturer & authorised representative

Manufacturer

Name: Ivalmed S.L.
SRN: ES-MF-000000634
Country: Spain
Email: gestion@ivalmed.com

Variants by status

UDI-DI variants

129 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01HV43SQYZEEJ3XFG9R51PK0FD

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

IV789-02-0408435760835579
IV789-02-0908435760838761
IV794-98-0108435760836002
IV794-9808435760808504

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