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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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DRS-215 — 32 UDI-DI variants, MDR (MEDICAL DEVICES GROUP S.R.L.)

MD Atlas
MEDICAL DEVICES GROUP S.R.L.

Data from EUDAMED, last updated May 30, 2026

DRS-215

805330332DRSEX

32 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: MEDICAL DEVICES GROUP S.R.L.

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Device characteristics

Active device

Identity & classification

Basic UDI-DI: 805330332DRSEX
Device name: DRS-215
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Mar 2, 2026

Manufacturer & authorised representative

Manufacturer

Name: MEDICAL DEVICES GROUP S.R.L.
SRN: IT-MF-000051612
Country: Italy
Email: t.delmonte@mdg-srl.com
Phone: +3905441826013

Variants by status

UDI-DI variants

32 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01KJQKRBTWEQC3KP95N63SJK8A

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

DRS-218/S/VP80533033204146
DRS-218/S/VP-TV80533033204382
DRS-218/TV80533033201862
DRS-218P/S-TV80533033204528
DRS-218P/S/VP80533033204832
DRS-218P/S/VP-TV80533033204764
DRS-218P/TV80533033201930

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