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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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Skin regenerating solution through… — 1 UDI-DI variant, MDD

MD Atlas
Dermoaroma Italy srl

Data from EUDAMED, last updated May 31, 2026

Skin regenerating solution through peeling

B-08056585951840

1 UDI-DI variant

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

Legislation: MDD [Directive 93/42/EEC on medical devices]
Risk class: Class IIb
Manufacturer: Dermoaroma Italy srl

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Device characteristics

No device characteristics flagged

Legacy certificates

Certificate number: 0425-MED-004441-00
Type: refdata.legacy.mdd-certificate-type.ii-excluding-4
Notified body: ICIM S.P.A. (0425)
Validity: May 26, 2024

Identity & classification

Basic UDI-DI: B-08056585951840
Device name: Skin regenerating solution through peeling
Device model: 5 ml vial
Issuing agency: EUDAMED
Legislation: MDD [Directive 93/42/EEC on medical devices]
Risk class: Class IIb
Version date: May 22, 2026

Manufacturer & authorised representative

Manufacturer

Name: Dermoaroma Italy srl
SRN: IT-MF-000034895
Country: Italy
Email: dermosrl@dermoaroma.com
Phone: 00390813207892

Variants by status

UDI-DI variants

1 UDI-DI variant

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Applied filters

basicUdiUlid01KS8B7P4T45SPGCN3Y3E0ERCS

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

CER00108056585951840