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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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CABESTRILLO CYMAN — 5 UDI-DI variants, MDR (EUROPODEX S.L.)

MD Atlas
EUROPODEX S.L.

Data from EUDAMED, last updated May 30, 2026

CABESTRILLO CYMAN

84370088420074Y

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: EUROPODEX S.L.

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 84370088420074Y
Device name: CABESTRILLO CYMAN
Device model: E2135,E2146,E2140S,EE2140M,E2140L,E2145
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: May 27, 2026

Manufacturer & authorised representative

Manufacturer

Name: EUROPODEX S.L.
SRN: ES-MF-000042401
Country: Spain
Email: info@europodex.com
Phone: +34 9 8599 08 33

Variants by status

UDI-DI variants

5 UDI-DI variants

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Applied filters

basicUdiUlid01KSAQXB9QZDTC4MJEHK81B7J4

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

E214608437008842608
E2140M08437008842622
E23508437008842592
E2140L08437008842639
E2140S08437008842615