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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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ETC 70S — 1 UDI-DI variant, MDR (DMED DI D IMPRIMA ANGELO)

MD Atlas
DMED DI D IMPRIMA ANGELO

Data from EUDAMED, last updated May 31, 2026

ETC 70S

805517623ETC70S9H

1 UDI-DI variant

MDR [Regulation (EU) 2017/745 on medical devices]Class I

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Manufacturer: DMED DI D IMPRIMA ANGELO

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 805517623ETC70S9H
Device name: ETC 70S
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Jun 5, 2025

Manufacturer & authorised representative

Manufacturer

Name: DMED DI D IMPRIMA ANGELO
SRN: IT-MF-000032812
Country: Italy
Email: angelo.dimprima@dmed.it
Phone: +393479585419

Variants by status

UDI-DI variants

1 UDI-DI variant

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Export results

Applied filters

basicUdiUlid01JX0DNXNXDPT51P8FH805QAKM

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

ETC 70S80551762300670