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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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Ophthalmology Custom Pack – MDN 1204 — 7 UDI-DI variants, MDR

MD Atlas
Delta Med SPA

Data from EUDAMED, last updated May 31, 2026

Ophthalmology Custom Pack – MDN 1204

8032248903019X

7 UDI-DI variants

MDR [Regulation (EU) 2017/745 on medical devices]Class IIa

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Manufacturer: Delta Med SPA

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 8032248903019X
Device name: —
Device model: Ophthalmology Custom Pack – MDN 1204
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: Dec 19, 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

7 UDI-DI variants

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Applied filters

basicUdiUlid01KCVJ6DX64G9K7PQMZ7J202GT

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

Custom pack FACO 2 private08032248903050
Custom pack for "Policlinico Modena"08032248903029
Custom pack for ophthalmology surgery08032248903074
Intravitreal custom pack08032248903081
Spinal anesthesia custom pack08032248903067
Spinal anesthesia custom pack08032248903036
Spinal kit08032248903043