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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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KIT ORTOPEDICO — 58 UDI-DI variants, MDR (NEW MEDICAL SERVICE SRL)

MD Atlas
NEW MEDICAL SERVICE SRL

Data from EUDAMED, last updated May 31, 2026

KIT ORTOPEDICO

805758735274108SK10KQ3

58 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: NEW MEDICAL SERVICE SRL

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UDI-DI variants

58 UDI-DI variants

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Applied filters

basicUdiUlid01KADPCHFTC4KE97V14STDHDVE

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

805758735294908057587352949
805758735295608057587352956
805758735296308057587352963
805758735297008057587352970
805758735298708057587352987
805758735299408057587352994
805758735300708057587353007
805758735301408057587353014
805758735302108057587353021
805758735303808057587353038
805758735314408057587353144
805758735315108057587353151
805758735316808057587353168
805758735317508057587353175
805758735318208057587353182
805758735319908057587353199
805758735320508057587353205
805758735321208057587353212
805758735322908057587353229
805758735274108057587352741
805758735275808057587352758
805758735276508057587352765
805758735277208057587352772
805758735278908057587352789
805758735279608057587352796

1 2 3

Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 805758735274108SK10KQ3
Device name: KIT ORTOPEDICO
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Nov 19, 2025

Manufacturer & authorised representative

Manufacturer

Name: NEW MEDICAL SERVICE SRL
SRN: IT-MF-000034543
Country: Italy
Email: info@flebysan.it
Phone: +39425474993

Variants by status