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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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Set in TNT e PE - Arthroscopy — 1 UDI-DI variant, MDR (Delta Med SPA)

MD Atlas
Delta Med SPA

Data from EUDAMED, last updated May 31, 2026

Set in TNT e PE - Arthroscopy

803224878001AJ

1 UDI-DI variant

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: 803224878001AJ
Device name: —
Device model: Set in TNT e PE - Arthroscopy
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Feb 6, 2026

Manufacturer & authorised representative

Manufacturer

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

Variants by status

UDI-DI variants

1 UDI-DI variant

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Export results

Applied filters

basicUdiUlid01KGSM5DP839JTEVGNM82BE588

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

Arthroscopy set08032248780026