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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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Rayvolve — 14 UDI-DI variants, MDR (AZmed)

MD Atlas
AZmed

Data from EUDAMED, last updated May 19, 2026

Rayvolve

3770018071008VP

14 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: AZmed

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 3770018071008VP
Device name: Rayvolve
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: Oct 8, 2024

Manufacturer & authorised representative

Manufacturer

Name: AZmed
SRN: FR-MF-000014277
Country: France
Email: Julien@azmed.co
Phone: + 33 6 49 69 78 59

Variants by status

UDI-DI variants

14 UDI-DI variants

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Applied filters

basicUdiUlid01GWSGHX6KH9DXBHB6QWJ72GGV

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

Rayscan37700180711522
Rayscan37700180711690
Rayscan37700180711768
Rayvolve37700180710082
Rayvolve37700180711386
Rayvolve37700180711454
Rayvolve37700180712062
Rayvolve - On-premise (Version 5)37700180711140
Rayvolve37700180710846
Rayvolve37700180711836
Rayvolve37700180711218
Rayvolve - VM/Cloud (Version 5)37700180710914
Rayvolve37700180711904
Rayvolve - Full cloud (Version 5)37700180711072