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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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CUBRE ESCAYOLA — 9 UDI-DI variants, MDR (MARTÍN BALART TARRIDA)

MD Atlas
MARTÍN BALART TARRIDA

Data from EUDAMED, last updated May 23, 2026

CUBRE ESCAYOLA

8437028213TF012G

9 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: MARTÍN BALART TARRIDA

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 8437028213TF012G
Device name: CUBRE ESCAYOLA
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Apr 24, 2026

Manufacturer & authorised representative

Manufacturer

Name: MARTÍN BALART TARRIDA
SRN: ES-MF-000044818
Country: Spain
Email: martibalart@gmail.com

Variants by status

UDI-DI variants

9 UDI-DI variants

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Applied filters

basicUdiUlid01KPZJ4DR6G9DT2FKVJ42GRQZX

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

MB001408437028213143
MB001108437028213112
MB001508437028213150
MB001208437028213129
MB001608437028213167
MB001308437028213136
MB001708437028213174
MB000908437028213099
MB001008437028213105