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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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CUSCINI MEDICALI PER POSIZIONAMENTO — 16 UDI-DI variants, MDR

MD Atlas
Service Med Srl

Data from EUDAMED, last updated May 31, 2026

CUSCINI MEDICALI PER POSIZIONAMENTO

805572850POSSMIQV

16 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: Service Med Srl

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 805572850POSSMIQV
Device name: CUSCINI MEDICALI PER POSIZIONAMENTO
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Apr 15, 2026

Manufacturer & authorised representative

Manufacturer

Name: Service Med Srl
SRN: IT-MF-000021629
Country: Italy
Email: info@servicemed.it
Phone: +390456717441

Variants by status

UDI-DI variants

16 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01KP8HMF2JXJDKBSTYWT2QGAG2

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

TI02010708055728500358
TI02011108055728500402
TI02010608055728500341
TI02010908055728500372
TI20109L08055728500389
TI02011508055728500440
TI02010108055728500297
TI02011308055728500426
TI02010808055728500365
TI02011408055728500433
TI02010208055728500303
TI02010308055728500310
TI02010508055728500334
TI02010408055728500327
TI02011008055728500396
TI02011208055728500419