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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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Not sterile Adapters for Enteral… — 8 UDI-DI variants, MDR (Cedic srl)

MD Atlas
Cedic srl

Data from EUDAMED, last updated May 30, 2026

Not sterile Adapters for Enteral Applications

805609372TD00182

8 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: Cedic srl

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 805609372TD00182
Device name: Not sterile Adapters for Enteral Applications
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Mar 27, 2025

Manufacturer & authorised representative

Manufacturer

Name: Cedic srl
SRN: IT-MF-000019323
Country: Italy
Email: quality@cedicbio.com

Variants by status

UDI-DI variants

8 UDI-DI variants

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Applied filters

basicUdiUlid01JDMH1HN737T3GM68X6QRMMM6

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

F0012708056093721676
7149 0008056093720723
58982808056093721331
F0010608056093720297
F0012508056093721645
F0013308056093720266
H93842907EN08056093720099
G 4498908056093721096