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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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BioRePeelCl3 — 2 UDI-DI variants, MDR (CMED AESTHETICS S.P.A.)

MD Atlas
CMED AESTHETICS S.P.A.

Data from EUDAMED, last updated May 31, 2026

BioRePeelCl3

805253618BRPCL3BL

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: CMED AESTHETICS S.P.A.

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Device characteristics

Incorporates a medicinal product

Identity & classification

Basic UDI-DI: 805253618BRPCL3BL
Device name: BioRePeelCl3
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: Mar 30, 2026

Manufacturer & authorised representative

Manufacturer

Name: CMED AESTHETICS S.P.A.
SRN: IT-MF-000012370
Country: Italy
Email: l.gervasi@cmedaesthetics.com

Variants by status

UDI-DI variants

2 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01KMJAGYXN9VHCQWE09VAWSXF5

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

PF.0005108052536181922
PF.0005708052536181939