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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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SPONDE UNIVERSALI — 5 UDI-DI variants, MDR (K S P Italia S.r.l.)

MD Atlas
K S P Italia S.r.l.

Data from EUDAMED, last updated May 31, 2026

SPONDE UNIVERSALI

805577318ACC-LETTOSPOND3

5 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: K S P Italia S.r.l.

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 805577318ACC-LETTOSPOND3
Device name: SPONDE UNIVERSALI
Device model: SPONDE UNIVERSALI
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Mar 19, 2026

Manufacturer & authorised representative

Manufacturer

Name: K S P Italia S.r.l.
SRN: IT-MF-000009316
Country: Italy
Email: ksp@kspitalia.com

Variants by status

UDI-DI variants

5 UDI-DI variants

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Applied filters

basicUdiUlid01KM2YH0H6K5S5J5JCKPVWVTNQ

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

A9151A08055773182943
A9121C08055773182912
A915108055773182936
A9121I08055773182905
A9132MI08055773182929