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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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Cuña sanitaria — 6 UDI-DI variants, MDR (ENVASES FARMACÉUTICOS, S.A.)

MD Atlas
ENVASES FARMACÉUTICOS, S.A.

Data from EUDAMED, last updated May 23, 2026

Cuña sanitaria

8431785UDI-DI-016F

6 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: ENVASES FARMACÉUTICOS, S.A.

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 8431785UDI-DI-016F
Device name: Cuña sanitaria
Device model: Cuña sanitaria
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Apr 20, 2022

Manufacturer & authorised representative

Manufacturer

Name: ENVASES FARMACÉUTICOS, S.A.
SRN: ES-MF-000000902
Country: Spain
Email: info@enfa.es
Phone: +34 916 580 936

Variants by status

UDI-DI variants

6 UDI-DI variants

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basicUdiUlid01FHWGSMADY3VHSZ70187HA7NS

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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

C1308470001987761
C1108431785003115
C1208432153000040
C0108431785003016
C1408430321723678
C0608430321723685