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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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VENDA CREPÉ- VENDA CREPÉ SUPERIOR — 10 UDI-DI variants, MDR

MD Atlas
FARMABAN s.a.

Data from EUDAMED, last updated May 23, 2026

VENDA CREPÉ- VENDA CREPÉ SUPERIOR

8428012crepeLS

10 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: FARMABAN s.a.

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 8428012crepeLS
Device name: VENDA CREPÉ- VENDA CREPÉ SUPERIOR
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Nov 11, 2022

Manufacturer & authorised representative

Manufacturer

Name: FARMABAN s.a.
SRN: ES-MF-000004713
Country: Spain
Email: farmaban@farmaban.com
Phone: 938789507

Variants by status

UDI-DI variants

10 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01GHH9KJVZXK4HHB21Z2H25V10

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

122608428012012262
122208428012012224
122008428012012200
122408428012012248
122808428012012286
120608428012012064
120208428012012026
120008428012012002
120408428012012040
120808428012012088