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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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Restylane Volyme — 1 UDI-DI variant, MDD (Q-Med AB)

MD Atlas
Q-Med AB

Data from EUDAMED, last updated May 31, 2026

Restylane Volyme

B-012089LS

1 UDI-DI variant

MDD [Directive 93/42/EEC on medical devices]Class III

Legislation: MDD [Directive 93/42/EEC on medical devices]
Risk class: Class III
Manufacturer: Q-Med AB

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Device characteristics

ImplantableIncorporates a medicinal product

Clinical investigations

Registered: No

Registered: No

Investigation number: NCT01545557
Registered: No
Countries: Brazil

Investigation number: NCT03289052
Registered: No
Countries: China

Investigation number: NCT03700047
Registered: No
Countries: United States

Investigation number: NCT04638816
Registered: No
Countries: Canada

Investigation number: NCT05691972
Registered: No
Countries: United States

Legacy certificates

Certificate number: 2021098CE13
Type: refdata.legacy.mdd-certificate-type.ii-excluding-4
Notified body: DEKRA Certification B.V. (0344)
Validity: Dec 31, 2027

Certificate number: 2021098DE26
Type: refdata.legacy.mdd-certificate-type.ii-4
Notified body: DEKRA Certification B.V. (0344)
Validity: Dec 31, 2027

Identity & classification

Basic UDI-DI: B-012089LS
Device name: Restylane Volyme
Issuing agency: EUDAMED
Legislation: MDD [Directive 93/42/EEC on medical devices]
Risk class: Class III
Version date: Apr 22, 2026

Manufacturer & authorised representative

Manufacturer

Name: Q-Med AB
SRN: SE-MF-000008549
Country: Sweden
Email: info.q-med@galderma.com

Variants by status

UDI-DI variants

1 UDI-DI variant

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Export results

Applied filters

basicUdiUlid01KPTQR2KP7ABQ84GK0RP0G24T

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

Restylane VolymeD-012089LS