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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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DIVA ancillary — 16 UDI-DI variants, MDR (SC MEDICA)

MD Atlas
SC MEDICA

Data from EUDAMED, last updated May 19, 2026

DIVA ancillary

377001950357006DQ

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: SC MEDICA

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Device characteristics

Reusable

Identity & classification

Basic UDI-DI: 377001950357006DQ
Device name: DIVA ancillary
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Apr 23, 2026

Manufacturer & authorised representative

Manufacturer

Name: SC MEDICA
SRN: FR-MF-000002722
Country: France
Email: info@sc-medica.com

Variants by status

UDI-DI variants

16 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01KP870VDGVVVS6JZRKSSAK5NX

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

57.006.XXE03760418040063
57.006.XXE03760418040025
57.006.XX03760418040056
57.006.XX03760418040131
57.006.XXE03760418040100
57.007.00-MO03760418040148
57.006.XXE03760418040001
57.006.XX03760418040070
57.006.XX03760418040094
57.006.XX03760418040032
57.006.XXE03760418040087
57.007.0003760418040155
57.006.XXE03760418040124
57.006.XX03760418040018
57.006.XX03760418040117
57.006.XXE03760418040049