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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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Lumi Referenced — 1 UDI-DI variant, MDR (Augmedit B.V.)

MD Atlas
Augmedit B.V.

Data from EUDAMED, last updated May 30, 2026

Lumi Referenced

87208926176LumiRef8J

1 UDI-DI variant

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

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIb
Manufacturer: Augmedit B.V.

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Device characteristics

Active device

Legacy certificates

Certificate number: SCAR-8.2.1.4
Type: refdata.certificate-mdr-type.quality-management-system
Notified body: Scarlet NB B.V. (3022)
Validity: May 26, 2026 → Oct 6, 2030

Identity & classification

Basic UDI-DI: 87208926176LumiRef8J
Device name: Lumi Referenced
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIb
Special device type: refdata.special-mdr-device-type.software
Version date: Jan 16, 2026

Manufacturer & authorised representative

Manufacturer

Name: Augmedit B.V.
SRN: NL-MF-000045948
Country: Netherlands
Email: info@augmedit.com
Phone: +31 617 1010 94

Variants by status

UDI-DI variants

1 UDI-DI variant

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Export results

Applied filters

basicUdiUlid01KF2XZ2T49Y3NRVAYX63JHHJ4

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

Lumi Referenced08720892617620