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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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Enteral drainage bags — 10 UDI-DI variants, MDR

MD Atlas
HMC PREMEDICAL S.P.A.

Data from EUDAMED, last updated May 31, 2026

Enteral drainage bags

805367629TD009ENTN1sAZ

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: HMC PREMEDICAL S.P.A.

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 805367629TD009ENTN1sAZ
Device name: Enteral drainage bags
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: May 15, 2026

Manufacturer & authorised representative

Manufacturer

Name: HMC PREMEDICAL S.P.A.
SRN: IT-MF-000029438
Country: Italy
Email: info@hmcgroup.it
Phone: +39053522704

Variants by status

UDI-DI variants

10 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01KRNF5D89A7ZWR523PQX14P29

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

MED251L18053676299574
MED501L18053676299581
MED50L18053676299505
MED51L18053676299550
MED1000L18053676299543
MED1001L18053676299598
MED250L18053676299529
MED101L18053676299567
MED500L18053676299536
MED100L18053676299512