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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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Gynecology Set — 11 UDI-DI variants, MDR (Delta Med SPA)

MD Atlas
Delta Med SPA

Data from EUDAMED, last updated May 31, 2026

Gynecology Set

803224877001AB

11 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: Delta Med SPA

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 803224877001AB
Device name: —
Device model: Gynecology Set
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Dec 5, 2025

Manufacturer & authorised representative

Manufacturer

Name: Delta Med SPA
SRN: IT-MF-000027962
Country: Italy
Email: info@numantec.eu

Variants by status

UDI-DI variants

11 UDI-DI variants

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Applied filters

basicUdiUlid01K4CBKQ8FD3DRQ6S1PYHQPPSX

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

Cesarean set08032248770102
Cesarean surgery set08032248770041
Complete hip kit08032248770027
Extremity set with gowns08032248770058
Gynecology open standard kit08032248770119
Gynecology standard kit for cesarean delivery08032248770126
Natural delivery set08032248770096
Set for T.U.R.08032248770034
SET PARTO CESAREO08032248770072
SET PARTO SPONTANEO08032248770065
urogynecological set08032248770089