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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 medicazione generica — 4 UDI-DI variants, MDR (D.R.M. S.R.L.)

MD Atlas
D.R.M. S.R.L.

Data from EUDAMED, last updated May 31, 2026

Kit medicazione generica

805959152KITMG1SYJ

4 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: D.R.M. S.R.L.

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 805959152KITMG1SYJ
Device name: Kit medicazione generica
Device model: Kit medicazione generica sterili
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Mar 26, 2026

Manufacturer & authorised representative

Manufacturer

Name: D.R.M. S.R.L.
SRN: IT-MF-000027115
Country: Italy
Email: info@drmsrl.it
Phone: +390386734312

Variants by status

UDI-DI variants

4 UDI-DI variants

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Applied filters

basicUdiUlid01KMNAKVHK9E9WZTRZY6ZG0SFD

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

GDR/MED/SM08059591526729
DR/I.P.D./308059591526330
DR 2/2 TK08059591525159
DR 61/CC08059591524336