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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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Sleeve — 60 UDI-DI variants, MDR (3DIEMME srl)

MD Atlas
3DIEMME srl

Data from EUDAMED, last updated May 30, 2026

Sleeve

805003883SLVJJ

60 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: 3DIEMME srl

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 805003883SLVJJ
Device name: Sleeve
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Dec 13, 2022

Manufacturer & authorised representative

Manufacturer

Name: 3DIEMME srl
SRN: IT-MF-000016005
Country: Italy
Email: support@3diemme.it

Variants by status

UDI-DI variants

60 UDI-DI variants

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Applied filters

basicUdiUlid01GM5EEF3QDST9AQRBXTBVPA6W

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

3DM00604CAD11.1018050038830130
3DM00605AZ48.1018050038833155
3DM006053iLARGE.1018050038830215
3DM00605NBL.RP.1018050038830635
3DM00605AZTC50.1018050038834428
3DM00605STR.1018050038830734
3DM00605ZIMB.1018050038833025
3DM00604CAD3.1018050038830154
3DM00605NBL.WP.1018050038830642
3DM00604CAD0.1018050038830093

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