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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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Surgical Guide — 70 UDI-DI variants, MDR (3DIEMME srl)

MD Atlas
3DIEMME srl

Data from EUDAMED, last updated May 30, 2026

Surgical Guide

8050038833DMCD

70 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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UDI-DI variants

70 UDI-DI variants

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Applied filters

basicUdiUlid01GM5DN21JJMB37DBXKFB2741J

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

3DCAD00015S08050038833103
ICEU-BBGDPRNT-I1-SA08050038832885
ICEU-APGDPRNT-I1-SA08050038832908
ICEU-APGDPRNT-I2-SW08050038832816
ICEU-GDPRNT-I3-SA08050038832946
ICEU-GDPRNT-I1-SA08050038832953
ICEU-BBGDPRNT-I2-SW08050038832793
ICEU-BBGDPRNT-I1-SW08050038832786
3DCAD00010S08050038832229
ICEU-APGDPRNT-I2-SA08050038832915
ICEU-APGDPRNT-I1-SW08050038832809
3DCAD00017I08050038832304
3DCAD00015I08050038833097
3DCAD00011I08050038832236
ICEU-APGDPRNT-I3-SA08050038832878
3DCAD00002S08050038830683
3DENDO0002S08050038832380
3DCAD00003S08050038830744
ICEU-BRGDPRNT-I2-SA08050038832847
3DCAD00010I08050038832212
3DCAD00001S08050038833370
3DCAD00009I08050038832199
3DM00126I-SLV08050038832700
3DCAD00006I08050038832007
3DCAD00007I08050038832151

1 2 3

Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 8050038833DMCD
Device name: Surgical Guide
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