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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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Hybrid Viewer — 2 UDI-DI variants, MDR (Hermes Medical Solutions AB)

MD Atlas
Hermes Medical Solutions AB

Data from EUDAMED, last updated May 30, 2026

Hybrid Viewer

085987300600168

2 UDI-DI variants

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

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Manufacturer: Hermes Medical Solutions AB

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Device characteristics

No device characteristics flagged

Legacy certificates

Certificate number: 28620167501-01
Type: refdata.certificate-mdr-type.quality-management-system
Notified body: Intertek Medical Notified Body AB (2862)
Validity: Mar 8, 2024 → Oct 3, 2028

Identity & classification

Basic UDI-DI: 085987300600168
Device name: Hybrid Viewer
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Special device type: refdata.special-mdr-device-type.software
Version date: Feb 29, 2024

Manufacturer & authorised representative

Manufacturer

Name: Hermes Medical Solutions AB
SRN: SE-MF-000023032
Country: Sweden
Email: info@hermesmedical.com

Variants by status

UDI-DI variants

2 UDI-DI variants

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basicUdiUlid01HQTHQHSZGVE0MDJP3RSWSGWW

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

0085987300618900859873006189
0085987300624000859873006240