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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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FAJA ELÁSTICA FLEMING TUBULAR — 5 UDI-DI variants, MDR

MD Atlas
Fleming Comercial, S.A.

Data from EUDAMED, last updated May 23, 2026

FAJA ELÁSTICA FLEMING TUBULAR

8426828fajatubular4E

5 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: Fleming Comercial, S.A.

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 8426828fajatubular4E
Device name: FAJA ELÁSTICA FLEMING TUBULAR
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Oct 19, 2022

Manufacturer & authorised representative

Manufacturer

Name: Fleming Comercial, S.A.
SRN: ES-MF-000004259
Country: Spain
Email: fleming-sa@fleming-sa.com
Phone: +34934902946

Variants by status

UDI-DI variants

5 UDI-DI variants

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Applied filters

basicUdiUlid01G10KRRHVSM0P2SW7C01A0E0K

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

220120108470003501163
220120208470003503976
220120308470003813761
220120408470003814836
220120508470003815178